173 Biotechnologist jobs in Singapore

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Direct message the job poster from ESCO ASTER PTE LTD

Esco Lifesciences Group is Singapore’s most globalized life sciences company, with annual revenues close to SGD 200M and global operations in over 42 locations and 26 direct countries across North America, Europe, Asia, Oceania.

Esco Aster Pte Ltd is an affiliate of Esco Lifesciences Group and was first incorporated in 2017.

Esco Aster is a contract research development and manufacturing organization founded and deeply rooted by scientists enabling fellow scientists to translate their bench work into commercially available products at affordable prices.

Our scientific work is in emerging and frontier biology utilizing cells as a final product or deriving products from cells which often we use cells as the factory to derive our target product.

Our first commercial breakthrough success is Esco Aster is commercially first in class being first in the world to be certified for cultivated/cell-based meat to FSSC 22000 and by a competent food regulatory body.

We are first in the region to operate an end-to-end integrated full cell line creation/immortalization or engineered cell line, cell culture process development, analytical development for stem cells and exosomes with full cGMP Capabilities from Drug Substance and small-scale fill & finish for final Cell Therapy Product.

The work we do creates a remarkable and lasting impact on our world. We offer you an opportunity to be part of this exciting journey to own your career and firsthand exposure to new emerging modalities supporting translational sciences.

Join us as we redefine BioSolutions for One World and One Health for the current and future generations to come.

One World Biosolutions for One Health.

Who we’re looking for

Physical / Mental Requirements / Work Environment:

• Strong leadership and communication skills.
• Ability to stay focused under pressure and adapt proactively.
• Critical thinker with a systematic and meticulous approach.
• Curious and self-motivated to stay updated on cell/gene therapy and emerging technologies.
• Committed to safety, quality, compliance, and timely delivery.
• Cleanroom and GMP manufacturing settings.
• Requires standing for long periods, working with sterile systems, and wearing full gowning/PPE.
• May engage in overtime during campaign activities or urgent troubleshooting.

The Scope

To support the successful technology transfer, manufacturing execution, and commercial readiness of cell and gene therapy products in a cGMP environment, ensuring compliance, efficiency, and delivery excellence throughout the product lifecycle.

Primary work location: Ayer Rajah Crescent, Singapore

Job Responsibilities

• Collaborate with internal/external stakeholders including QA, QC, MSAT, and commercial teams.
• Serve as Manufacturing Subject Matter Expert (SME) during audits, inspections, and due diligence.
• Involve in technology transfers (internal and external) and commissioning, qualification (C&Q) activities.
• Involve in Process Performance Qualification (PPQ), Aseptic Process Simulations (APS), and engineering/pilot runs.
• Support in cell culture, purification, and fill-finish operations in a single-use, aseptic, cGMP facility.
• Help in Ensuring readiness of raw materials, equipment, and team for autologous/ allogeneic campaigns.
• Ensure accurate and timely data entry in digital records, maintaining compliance with Good Documentation Practices (GDP).
• Author, review, and manage cGMP documentation: SOPs, batch records, risk assessments, protocols, etc.
• Support with manufacturing change control, deviation investigations and implement CAPAs.
• Support the implementation of electronic batch records.
• Undertake other tasks as assigned by the management based on project needs.

Requirements

• Minimum Bachelor’s Degree in Biotechnology related disciplines, Chemical Engineering, Pharmaceutical Science or relevant discipline with 2 years or more experience in a cGMP/aseptic environment in biologics or cell and gene therapy.
• Minimum of 2-4 years in cGMP Biologics or cell and gene therapy manufacturing with relevant industry knowledge, hands on equipment experience and technical expertise. Upstream Manufacturing Process.
• Experience in Downstream and Upstream Manufacturing Process and/or Process Support services.
• Strong knowledge of cGMP practices and global regulatory requirements such as USFDA GMP, EU GMP, HSA GMP and PIC/S GMP.
• Proficient in MS Office Suite (Microsoft Word, PowerPoint, Excel).
• Able to work independently and task oriented in a dynamic environment.
• Strong team player with a strong set of interpersonal skills.
• Excellent written and verbal communication skills.
• Experience in working in cell and gene therapy manufacturing is an added advantage.

Apply now by submitting a Cover Letter and CV to .

Seniority level

• Seniority level Associate

Employment type

• Employment type Full-time

Job function

• Job function Research, Manufacturing, and Analyst

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Technical Specialist 3 (Deviation Investigation) Medical Technologist I (Histology Lab experience preferred) Scientist for Advanced Photonics (Photonic Computing), IME Scientist (Social Sciences, Human Development), IHDP Development Scientist, Digital Supply Chain, ARTC Section Lead, Logistics & Warehouse (CGT) Manufacturing Biotechnologist Trainee - Train & Place Program Manufacturing Biotechnologist - Train and Place Manufacturing Biotechnologist - Train and Place Program Manufacturing Biotechnologist - Train & Place

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The incumbent will be involved in day-to-day support in biologics and vaccine manufacturing operation by providing operation/maintenance input and facilitate decision making. He/she will act as user representative/area owner in terms of technical transfer of process and product from R&D and CMC to GMP clinical manufacturing of different modalities and platforms to meet tech transfer objectives and timeline. He/she will commission first of its kind multiproduct cGMP manufacturing suites (mammalian, microbial suites) within project timeline and budget.

Job scope

RESPONSIBILITIES:

• Responsible in ensuring that the manufacturing activities are performed in accordance with EHS guidelines and in a cGMP-compliant manner.
• Provide input to operation and equipment in the tech transfer activities of new product/process.
• Draft, author and/or provide inputs in documentations such as facility fit assessment, user requirements, raw material identification, batch records, SOPs, and process recipes.
• To coordinate with relevant departments, stakeholders in tracking of operation progression to ensure project milestones are met.
• Perform and lead root cause analysis for operational related deviations and investigations using established problem-solving tools.
• Train and coach manufacturing team in process and equipment knowledge to ensure operations are conducted in a safe manner.
• Manage change controls and deviations of GMP runs for clinical manufacturing.
• Support process/equipment qualification/validation activities and studies.
• Front auditors during regulatory audits as the SMEs of the department.
• Perform cleaning of equipment and cleanrooms as and when necessary.

EDUCATION, BEHAVIOURAL COMPETENCIES AND SKILLS:

• Bachelor’s degree in a engineering/scientific discipline (Bio/chemical engineering/life science/biology/chemistry) with 2-6 years relevant industry experience.
• Plant start-up or commissioning and/or operational experience in biologics and/or vaccines
• Biological technology transfer experience will be an advantage
• Experience/knowledge of cGMP practices applicable to upstream/downstream virus manufacturing processes, process development is desirable
• Thorough knowledge of Good Documentation Practices (GDP) and Current Good Manufacturing Practices (cGMP)
• Well-organized and detail-oriented, with ability to effectively prioritize tasks with agility, eager to learn, interact and collaborate effectively with various stakeholders in a team environment and consistently demonstrate reliability and responsibility.
• Good team player with good working ethics, initiative, diplomacy, positive influencing abilities and drive.
• Good oral communication and demonstrable, exemplary writing skills.
• Experience with problem solving and statistical tools will be an advantage

Seniority level

• Seniority level Associate

Employment type

• Employment type Full-time

Job function

• Job function Engineering, Research, and Manufacturing
• Industries Research Services and Biotechnology Research

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**_About the job_**
Sanofi Manufacturing and Supply organization is preparing its future through an ambitious program named Modulus. The Modulus Project is at the cornerstone of Sanofi strategy as it aims at creating a new manufacturing concept consisting of a new generation of evolutive multi-product facilities, modular, adaptable and agile, leveraging new disruptive technologies, to better address vaccine business challenges as well as Specialty Care Biologics products. One of these two facilities is implemented in Singapore in a new Greenfield site, with a design identical to the one in Neuville (France). The facilities will also have highly digitalized and automated capabilities which is a key enabler for operations using technologies such as autonomous guided vehicles (AGVs), cobots and cloud systems.
This role will have the title of Biotechnologist, Manufacturing and will report to the Manager, Manufacturing. The successful candidate will be part of the pioneer batch of the manufacturing operations shift team who will directly participate in the Engineering and Product Validation Runs in the state-of-the-art facility.
The candidate will have a routine operational role consisting of the following:
+ Perform and complete ongoing commissioning and qualification activities of equipment, digital and automation related systems.
+ Execute routine GMP manufacturing activities in the manufacturing operations team in accordance with Process, Quality and Safety standards.
+ Perform general housekeeping of the manufacturing areas.
+ Support ongoing regulatory and audit readiness and preparation.
+ User of key digital and automation applications and software related to manufacturing systems such as ERP, MES, PCS, etc.
+ Participation in continuous improvement and optimization projects.
Sanofi Modulus Singapore is hiring for Biotechnologist, Manufacturing for the following teams:
+ Upstream Manufacturing Process
+ Downstream Manufacturing Process
+ Central Manufacturing Services (Media & Buffer, Logistics)
**Main responsibilities:**
+ Commissioning and Qualification Activities, Operational Readiness: perform and execute commissioning activities for manufacturing equipment and systems.
+ Support the documentation readiness for procedures, risk assessment and other training documents for the manufacturing equipment and systems.
+ Tech Transfer: Participate and complete all related trainings to perform the tech transfer runs.
+ cGMP Manufacturing Operations: Perform and participate in the Engineering Runs and other Product Validation Runs
**_About You_**
+ Degree in an Engineering or Science discipline
+ Starting job grade of the role will be commensurate with the applicant's highest education qualification and any other relevant experience.
+ Candidates with prior internships or industrial attachments in biopharmaceutical and biotechnology organizations would be advantageous. -
+ Self-starter and independent worker who can operate and perform in cross functional teams.
+ Possess strong analytical and critical thinking skills with the ability to problem solve and navigate through complexity and ambiguity.
+ Able to work in fast paced and dynamic conditions with tight timelines.
+ Good presentation and verbal communication skills who can adapt and tailor communication to various stakeholders.
+ Excellent technical writing skills
+ Team Player Biotechnologist will be working in a twelve-hour rotating shift pattern consisting of day and night shifts which will include weekend workdays when the facility is fully operational.
**Pursue** **_progress_** **, discover** **_extraordinary_**
Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.
Watch our ALL IN video ( and check out our Diversity Equity and Inclusion actions at sanofi.com ( !
Global Terms & Conditions and Data Privacy Statement ( is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering. We stand by the few who suffer from rare diseases and the millions with long-term chronic conditions.
With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe. Discover more about us visiting or via our movie We are Sanofi ( an organization, we change the practice of medicine; reinvent the way we work; and enable people to be their best versions in career and life. We are constantly moving and growing, making sure our people grow with us. Our working environment helps us build a dynamic and inclusive workplace operating on trust and respect and allows employees to live the life they want to live.
All in for Diversity, Equity and Inclusion at Sanofi - YouTube (

Today, Lonza remains a global leader in life sciences operating across five continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is dedicated people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of.

As a seasoned Biotechnologist at Lonza Cell & Gene Therapy business, you'll be part of our globally recognized network, driving the production of cell & gene treatments.

Join our outstanding high performance Coordinated Biologics team at our Tuas site in Singapore to gain unparalleled exposure to innovative biotechnology and innovation. Learn new skills and capabilities. Grow your career with us in manufacturing therapeutic proteins under cGMP conditions.

What you'll get:

• An agile career and dynamic working culture.
• An inclusive and ethical workplace.
• Compensation programs that recognize high performance.
• Daily company bus from the MRT location near your home to and from the Tuas site.
• Fully paid medical insurance, with the option to enroll family members at partially subsidized premiums.
• Shift allowances.

The full list of our global benefits can be also found on you'll do:

• Attains a thorough understanding of the principles of cGMP compliance aseptic techniques and clean room practices.
• Executes batch records, ensuring right-first time and accurate documentation.
• Maintains training status to perform required GMP tasks.
• Performs environmental monitoring during production.
• Performs suite support activities, e.g. equipment cleaning, housekeeping.
• Escalates non-routine situations (e.g. deviations, equipment alarms) per site procedure.
• Uses electronic systems to perform work (e.g. document management system (DMS), Lab Information Management System (LIMS), Trackwise).
• Reviews executed batch records and logbooks in an accurate and timely manner.
• Suggests and participates in continuous improvement initiatives.
• Assignee to Trackwise records (e.g. CAPAs).
• Perform any other duties as assigned by your Lead/ Manager.
• Gains thorough understanding of critical process parameters and operational parameters.
• Raises and follows through work notifications.
• Initiates, executes and follows through with change requests.
• Provides coaching and mentoring to junior members of the team.
• Inputs into investigation of complex technical problems, compliance failures.
• Performs process & equipment troubleshooting.
• May take on Lab-in-charge responsibilities.

What we're looking for:

• Degree or equivalent experience in a related Science/Engineering field.
• Technical knowledge of Biopharmaceutical processing is mandatory.
• Relevant work experience in a similar manufacturing industry or cleanroom environment preferred.
• Strong Knowledge of cGMP applications.
• Positive team-oriented demeanor.
• Strong communication and interpersonal skills.
• Willingness to perform a rotating 12-hour shift pattern.

Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the happiness that comes with improving lives all around the world. The happiness that comes with making a meaningful difference.

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of.

As a Biotechnologist at Lonza Cell & Gene Therapy business, you'll be part of our globally recognized network, driving the production of cell & gene treatments.

Join our best-in-class high performance Integrated Biologics team at our Tuas site in Singapore to gain unparalleled exposure to cutting-edge biotechnology and innovation. Learn new skills and capabilities. Grow your career with us in manufacturing therapeutic proteins under cGMP conditions.

What you'll get:

• An agile career and dynamic working culture.
• An inclusive and ethical workplace.
• Compensation programs that recognize high performance.
• Daily company bus from the MRT location near your home to and from the Tuas site.
• Fully paid medical insurance, with the option to enroll family members at partially subsidized premiums.
• Shift allowances.

The full list of our global benefits can be also found on you'll do:

• Acquires a detailed understanding of the principles of cGMP compliance, aseptic techniques, and clean room practices.
• Completes batch records, ensuring accurate and right-first-time documentation.
• Maintains training status to perform required GMP tasks.
• Performs environmental monitoring during production.
• Performs suite support activities, e.g. equipment cleaning, housekeeping.
• Advances non-routine situations (e.g. deviations, equipment alarms) per site procedure.
• Uses electronic systems to perform work (e.g. document management system (DMS), Lab Information Management System (LIMS), Trackwise).
• Reviews completed batch records and logbooks in an accurate and timely manner.
• Suggests and participates in continuous improvement initiatives.
• Assignee to Trackwise records (e.g. CAPAs).
• Perform any other duties as assigned by your Lead/ Manager.

What we're looking for:

• Degree or equivalent experience in a related Science/Engineering field.
• Open to fresh graduates.
• Knowledge of Biopharmaceutical processing is an added asset.
• Relevant work experience in a similar manufacturing industry or cleanroom environment preferred.
• Knowledge of cGMP applications.
• Positive team-oriented demeanor.
• Strong communication and interpersonal skills.
• Willing to perform a rotating 12-hour shift pattern.

Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the happiness that comes with improving lives all around the world. The happiness that comes with making a meaningful difference.

Roles & Responsibilities

Job Description

80%

• Perform loading and Operating of Autoclave

• Responsible for MFR (Manufacturing Formulation Record)/SOP creation and revision

• Perform monitoring for process and equipment performance during operation as per SOP/MFR, identify and report if there's any atypical events

• Support investigation to event and deviation

• Interface with other departments to resolve issues related to daily operations

• Actively support transfer of new processes and commission/validation of new projects

• Actively support Change Control management

10%

The individual will manage equipment and support facility related projects by

• Support routine safety and GMP walk down and responding to findings (If required)

• Support execution of Corrective/Preventive actions which identified (If required)

• Support change control activities which assigned (If required)

• Act as a SME for investigation and solution

• Liaise with other department for Corrective/Preventive actions which identified

• Support shift change/handover activities

10%

Staff Technical Training and Development

• Meet and maintain training requirements

• Complete assigned training on time

• Provide technical training for area personnel

• Provide input on training material development

• Deputize for shift supervisor's activities

• Provide annual performance self-assessment on development plan

• Responsibility to adhere to any applicable EHS requirements.

• Commitment to a fair and respectful relationship to others and behavior in accordance with Code of Conduct.

Education and Experience Requirements

• Min Degree in Biomedical Sciences / Chemical Engineering or related with up to three years of relevant experience in the biotechnology, pharmaceutical industry

• Demonstrate commitment to cGMP, EHS compliance aspects of clean-room and plant operation

• Able to take initiative with good problem solving skills

• Excellent team player with hands-on attitude

• Able to work on rotating shifts

• Ability to lift, pull or push equipment requiring up to 20kg

• Able to climb ladders and work on platforms

• Able to perform confine space entrant/attendant/Supervisor/Assessor (If required)

• Ability to read/understand Safety Data Sheet (SDS) and handle chemicals as per SOP

• Able to monitor and analyze processing parameters to identify atypical trends

• Able to support Continuous Improvement Projects

• Able to perform as a subject matter expert for equipment and/or systems

If you are interested in any of the positions, do kindly drop your most updated resume to

Thank You.

Leon Leong De Cong

R1551708

Recruit Express Pte Ltd (Healthcare & Lifesciences Division)

EA License: 99C4599

Tell employers what skills you have

Pharmaceutical Industry
Lifesciences
Healthcare
GMP
Investigation
Formulation
Biotechnology
Technical Training
Change Control
Team Player
Manufacturing
Chemical Engineering
Autoclave
EHS

Roles & Responsibilities

Location: Kranji (Walking distance from MRT, 5-min shuttle bus available)

Duration:

• 2x positions till 31 Mar 2026 (contract under RE)
• 2x positions for 6 months (contract under RE)

Salary:

• Degree: $3,500 basic (max $,500 with experience)
• Shift Allowance: + 800/month (only if on rotating shift)
• Nitec/Dip holders: From 2,200 (based on experience)

Shifts: Rotating 12-hour shifts (3/2/2/3 pattern – Day/Night, 7:30am/pm to 7:30pm/am)

Key Responsibilities:

• Perform manufacturing operations in Cell Culture & Purification
• Operate equipment and follow SOPs
• Record data in batch records/logbooks
• Maintain cleanroom & follow aseptic techniques
• Support equipment cleaning, maintenance & changeover
• Participate in technical training & continuous development

interested applicants send your updated CV to

Jocelyn Chan| Consultant | Recruit Express Pte Ltd (Healthcare & Lifescience)

Company EA Licence number : 99C4599

Personnel EA License: R1331820

Tell employers what skills you have

Ingredients
Troubleshooting
Quality Control
Housekeeping
Inventory
Healthcare
Cell Culture
Chemistry
Purification
Manufacturing Operations
Technical Training
Food Technology
Food Science
Laboratory
Manufacturing
Technical Support

About No deviation

At No deviation, we are dedicated to delivering patient-centric solutions that revolutionize the pharmaceutical landscape. As a dynamic expert in engineering consultancy, Commissioning Qualification Validation (CQV), and Quality, Compliance, and Regulatory services, we are looking for individuals who are excited to contribute to impactful projects and drive innovation.

We believe that great things happen when Empathy, Integrity, and Transparency guide our actions. That's why we foster a culture of collaboration, inclusion, and continuous development – empowering our team members to grow personally and professionally.

Position Overview

We are looking for a proactive and hands-on Biotechnologist to support brownfield facility expansion activities in a regulated biopharmaceutical environment. This role focuses on preparing manufacturing operations for startup, including equipment readiness, documentation review, mock runs, and supporting process validation and GMP transition.
You will work closely with Manufacturing, Process Engineering, CQV, and Quality teams to ensure a smooth handover from project to operations for areas such as upstream, downstream, media/buffer preparation, or formulation/fill depending on project scope.

Key Responsibilities

• Support equipment and facility readiness activities, including area walkthroughs, punch list closure, and the setup of preparation and production areas.
• Contribute to the development and review of batch records, standard operating procedures (SOPs), work instructions, and material/equipment lists.
• Assist in planning and executing mock runs, operator training sessions, and GMP simulations.
• Work closely with cross-functional teams to ensure processes, workflows, and documentation align with GMP and operational requirements.
• Support process verifications, sampling plans, and data collection activities during startup runs.
• Provide on-the-floor support during commissioning, qualification, and process validation phases.
• Perform basic troubleshooting and escalate technical issues to the appropriate teams when necessary.
• Ensure adherence to safety, environmental, and GMP regulations throughout all activities.
• Leverage experience in optimize downstream processes (e.g., filtration, chromatography, centrifugation) for large-scale production.

Required Qualifications

• Diploma or degree in Biotechnology, Life Sciences, Biochemical Engineering, or a related field
• 3-8 years of relevant experience in a biotech or biopharmaceutical GMP environment
• Exposure to facility startup, tech transfer, or brownfield/greenfield projects is an advantage
• Basic understanding of bioprocess operations (upstream, downstream, or support functions)
• Familiarity with cleanroom protocols, buffer/media prep, and GMP documentation
• Strong interpersonal, communication, and problem-solving skills
• Able to work independently and collaboratively in a fast-paced project environment

Why join us?

• Generous Leave Policy.
• Comprehensive Health & Wellness Coverage: Receive robust medical and dental coverage to support your health needs.
• Professional Development Opportunities: Access continuous learning programs and resources for career growth within the company.
• Inclusive Culture: Work in an environment where innovation, collaboration, and diverse perspectives are encouraged and celebrated.
• Shape the Future: Make a real difference in the pharmaceutical industry while advancing your career.

How to apply

Are you ready to play a key role in shaping the future of pharmaceutical solutions? If you're passionate about making an impact, we want you on our team!

Please submit your resume, outlining your qualifications and experience relevant to the role, here.

About No deviation

At No deviation, we are dedicated to delivering patient-centric solutions that revolutionize the pharmaceutical landscape. As a dynamic expert in engineering consultancy, Commissioning Qualification Validation (CQV), and Quality, Compliance, and Regulatory services, we are looking for individuals who are excited to contribute to impactful projects and drive innovation.

We believe that great things happen when Empathy, Integrity, and Transparency guide our actions. That's why we foster a culture of collaboration, inclusion, and continuous development empowering our team members to grow personally and professionally.

Position Overview

We are looking for a proactive and hands-on Biotechnologist to support brownfield facility expansion activities in a regulated biopharmaceutical environment. This role focuses on preparing manufacturing operations for startup, including equipment readiness, documentation review, mock runs, and supporting process validation and GMP transition.
You will work closely with Manufacturing, Process Engineering, CQV, and Quality teams to ensure a smooth handover from project to operations for areas such as upstream, downstream, media/buffer preparation, or formulation/fill depending on project scope.

Key Responsibilities

• Support equipment and facility readiness activities, including area walkthroughs, punch list closure, and the setup of preparation and production areas.
• Contribute to the development and review of batch records, standard operating procedures (SOPs), work instructions, and material/equipment lists.
• Assist in planning and executing mock runs, operator training sessions, and GMP simulations.
• Work closely with cross-functional teams to ensure processes, workflows, and documentation align with GMP and operational requirements.
• Support process verifications, sampling plans, and data collection activities during startup runs.
• Provide on-the-floor support during commissioning, qualification, and process validation phases.
• Perform basic troubleshooting and escalate technical issues to the appropriate teams when necessary.
• Ensure adherence to safety, environmental, and GMP regulations throughout all activities.
• Leverage experience in upstream operations such as cell culture, fermentation, and centrifugation, and apply knowledge of DeltaV and MES systems to support manufacturing processes.

Required Qualifications

• Diploma or degree in Biotechnology, Life Sciences, Biochemical Engineering, or a related field
• 3-8 years of relevant experience in a biotech or biopharmaceutical GMP environment
• Exposure to facility startup, tech transfer, or brownfield/greenfield projects is an advantage
• Basic understanding of bioprocess operations (upstream, downstream, or support functions)
• Familiarity with cleanroom protocols, buffer/media prep, and GMP documentation
• Strong interpersonal, communication, and problem-solving skills
• Able to work independently and collaboratively in a fast-paced project environment

Why join us?

• Generous Leave Policy.
• Comprehensive Health & Wellness Coverage: Receive robust medical and dental coverage to support your health needs.
• Professional Development Opportunities: Access continuous learning programs and resources for career growth within the company.
• Inclusive Culture: Work in an environment where innovation, collaboration, and diverse perspectives are encouraged and celebrated.
• Shape the Future: Make a real difference in the pharmaceutical industry while advancing your career.

How to apply

Are you ready to play a key role in shaping the future of pharmaceutical solutions? If you're passionate about making an impact, we want you on our team!

Please submit your resume, outlining your qualifications and experience relevant to the role, here.