Candidates with process engineering or biotechnology backgrounds and a systems-level mindset will find this role in a collaborative, cross-functional R&D and manufacturing environment in Cape Town.
Derived from job-description analysis by Serendipath's career intelligence engine.
Original posting from Watchmaker Genomics
Position: Process Development Associate
Focus Area: Formulations
Position Type: Full-Time Employee
Location: Cape Town, South Africa (on-site)
Experience: Minimum BSc/BEng in Process/Chemical Engineering with 0 - 2+ years relevant experience in process engineering or biotechnology
Company Summary
Watchmaker Genomics is a global life sciences company with R&D and Production facilities in Cape Town, South Africa, and headquarters in Boulder, Colorado. Our team is driven by a passion for innovation and a commitment to collaboration, creativity, and scientific rigour. We believe that the intersection of biology, engineering, and computer science offers exciting opportunities to develop novel technologies that advance research and enhance human health. We leverage our enzyme engineering and computational biology capabilities to develop products that support high-growth applications in genomics, molecular diagnostics, and personalised medicine.
Position Summary
We are seeking an R&D Associate to join our Process Development team in Cape Town, South Africa.
As part of the Process Development team, you will apply your expertise in process engineering to design and transfer reagent manufacturing processes. You will contribute directly in delivering high-quality, innovative products to our customers. In this highly collaborative role, you will work closely with various departments, including R&D, Production, IT, and Quality Assurance across our global sites.
Key Responsibilities
The Process Development team supports the transfer of new products from R&D to manufacturing. This involves translating product requirements into process specifications and developing efficient, scalable processes to meet these needs. After product launch, the team provides ongoing support for process updates to maintain product quality.
Specific responsibilities include:
Identifying critical process parameters (CPPs) that ensure critical-to-quality attributes (CQAs) are consistently achieved.
Assisting in developing or adapting processes to meet CPPs by investigating new methods, equipment and controls, and confirming suitability through experimentation.
Identifying opportunities for process streamlining, standardization, and alignment with industry best practices.
Planning and executing assigned project deliverables and proactively communicating status and outcomes.
Contributing to process, equipment, and computer systems validation, as well as material qualification, by establishing clear, testable specifications based on CPPs and CQAs, along with associated experimental planning.
Identifying and documenting process risks, assessing potential impacts, and developing appropriate mitigations.
Contributing to robust, rigorous experimental design for the development and testing of new processes and comprehensively document outcomes.
Having a working understanding of the ISO13485 standard and internal standard operating procedures (SOPs) to effectively apply these principles.
Supporting on-market products by investigating process-related issues through data trending, analysis, or experimentation.
Authoring and revising work instructions, batch record templates, and other production-facing documentation that are clear and concise to ensure reproducible results.
Preparing training materials and conducting classroom and on-the-job training of operators on new or revised procedures.
Required skills
Predisposition for systems-level thinking, as applied to designing and implementing robust, scalable processes for reagent manufacturing.
Demonstrated scientific excellence in technical work, written communication and presenting technical information to groups with various scientific backgrounds.
Adaptability, curiosity and ability to grasp and apply new concepts quickly.
Critical thinking and problem-solving skills.
Commitment to a culture of excellence and advocacy for continuous improvement.
Strong interpersonal skills and an excellent ability to drive results in multi-level, cross-functional teams.
Excellent organizational skills and outstanding attention to detail.
Strong personal task management skills and a high level of self-motivation.
Excellent written and verbal communication skills.
Advantageous skills
Technical understanding of and/or experience with:
PCR, next-generation sequencing (NGS) techniques, and basic protein biochemistry (e.g., physical properties, experimental methods, enzyme kinetics, etc.).
Mid-scale life science reagent manufacturing and scale-up.
Analytical measurement methods and assessing process capabilities, using statistical techniques such as Measurement Systems Analysis (MSA) or Gauge Repeatability & Reproducibility (Gauge R&R).
Designing and monitoring processes using statistical methods such as Design of Experiments (DOE) and Statistical Process Control (SPC).
General statistical techniques such as regression analysis and significance testing (e.g., Analysis of Variance (ANOVA), t-tests).
Risk management and hazard analysis frameworks or tools, such as Failure Modes and Effects Analysis (FMEA).
ISO 9001 and/or ISO 13485 standards or operating within a structured quality management system (QMS).
Requirements
BSc/BEng in Process/Chemical Engineering with 0 - 2+ years relevant experience in process engineering or biotechnology
OR
MSc in molecular biology/enzymology or related fields with 2+ years demonstrated industry experience in process development
Application Requirements
To apply for the position, please submit the following in a PDF format on watchmakergenomics.com:
Letter of motivation (upload where it says cover letter)
Resume or Curriculum vitae, highlighting relevant qualifications and experience
Applications without a Letter of Motivation will not be considered. Local candidates preferred.
If selected to participate in the interview process, the names and contact information of three professional references who are able to assess your suitability for the position in terms of the specified requirements will be requested.
To ensure your application is considered, please submit it by Friday, 23 October 2026. Please note that this position may close earlier if we receive a high volume of applications. We encourage you to apply as soon as possible.
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SOUTH AFRICA - WE ARE AN EQUAL OPPORTUNITY/AFFIRMATIVE ACTION EMPLOYER
Watchmaker Genomics is committed to being an equal opportunity employer and creating a culturally diverse environment. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability status, age, or veteran status or any other characteristics as protected by applicable law.
All applicants will be asked if currently eligible to work in South Africa; and if now or in the future will require visa sponsorship to continue working in South Africa.
This position may be subject to pre-employment checks, including driving history check, drug screening and a background check for any convictions directly related to its duties and responsibilities. All pre-employment checks will comply with all applicable laws.
Source: Watchmaker Genomics careers