118 Process Development jobs in South Africa

Watchmaker Genomics - Validation Lead Position Watchmaker Genomics is a global life science company with an R&D and Production facility in Cape Town, South Africa and head offices in Boulder, Colorado. Our team is passionate about innovation and values collaboration, creativity, and scientific rigor. We believe that the intersection of biology, engineering, and computer science presents exciting opportunities for developing novel technologies that promote research and improve human health. Watchmaker Genomics specializes in the design, development, and production of DNA- and RNA-modifying enzymes that enable high-growth applications in genomics, molecular diagnostics, and personalized medicine. We are inviting applications for a full-time Validation Lead position to be based in Cape Town, South Africa. This position reports to the Process Development Lead and will be responsible for the coordination of validation activities across our global sites. This is a highly collaborative position that involves working closely with members of other departments such as R&D, Production, IT, and Quality Assurance. The successful candidate will thrive in a dynamic, fast-paced working environment and contribute directly to our company culture and success. Duties & Responsibilities Responsibilities Validation lifecycle management: Managing the entire lifecycle of validation activities from initial planning through post-execution review and maintenance of validated status. Implement and manage execution of the company validation program: Develop and implement the validation strategy. Coordinate validation activities with relevant areas and external service providers. Oversee validation of: Infrastructure and Utilities Cleaning Equipment Software & Computer Systems (in collaboration with IT) Processes, including Shipping Test methods Author and maintain validation procedures & documents: Author and approve validation & project plans, protocols, and reports. Review qualification protocols and reports of third-party service providers. Provide technical expertise and training for validation activities: System risk assessments and required level of validation. Identification of user requirements. Project plans, protocols, and reports. Provide expertise related to relevant validation activities. Desired Experience & Qualification The following skills and experience are requirements for the position: Experience in planning and executing validation protocols - including process validation, computer systems validation, test method validation, and/or equipment qualification. Demonstrated ability to design and monitor systems using statistical methods such as Design of Experiments (DOE), Statistical Process Control (SPC), Regression Analysis, Analysis of Variance (ANOVA), and Gage Repeatability & Reproducibility (Gage R&R). ISO 13485, ISO 9001, and/or c GMP industry experience in Process Development, Quality Assurance, Quality Systems, Operations, or other related field. Broad technical knowledge of life science reagents, genomics, next-generation sequencing (NGS), PCR, and/or recombinant protein production are all highly desirable. Demonstrated scientific excellence in technical work, written communication, and presenting technical information to groups with various scientific backgrounds. The ability to multitask, perform consistently under pressure, and work without supervision. Strong interpersonal skills and an excellent ability to drive results in multi-level, cross-functional teams. Excellent organisational skills and outstanding attention to detail. Good communication and personal task management skills and a high level of self-motivation. Ability to determine project timelines and meet deadlines. Excellent written and verbal communication skills. Education and Experience An MSc in molecular biology, biochemistry or BEng Hons in Engineering or a related discipline is required. A minimum of 3 years in biotech or related industry is desirable, including positions with broad functional scope across research and development, technical transfers, manufacturing, quality control, and quality assurance. Certification or qualification as a validation engineer, such as Certified Validation Professional (CVP) or Certified Quality Validation Engineer (CQVE) is preferred. Interested? Application Procedure To apply for the position, please submit the following in PDF format on Indeed (Add Link here): Letter of motivation 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 3 references who are able to assess your suitability for the position in terms of the specified requirements will be requested. *** 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. #J-18808-Ljbffr

Watchmaker Genomics - Validation Lead Position Watchmaker Genomics is a global life science company with an R&D and Production facility in Cape Town, South Africa and head offices in Boulder, Colorado. Our team is passionate about innovation and values collaboration, creativity, and scientific rigor. We believe that the intersection of biology, engineering, and computer science presents exciting opportunities for developing novel technologies that promote research and improve human health. Watchmaker Genomics specializes in the design, development, and production of DNA- and RNA-modifying enzymes that enable high-growth applications in genomics, molecular diagnostics, and personalized medicine. We are inviting applications for a full-time Validation Lead position to be based in Cape Town, South Africa. This position reports to the Process Development Lead and will be responsible for the coordination of validation activities across our global sites. This is a highly collaborative position that involves working closely with members of other departments such as R&D, Production, IT, and Quality Assurance. The successful candidate will thrive in a dynamic, fast-paced working environment and contribute directly to our company culture and success. Duties & Responsibilities Responsibilities Validation lifecycle management: Managing the entire lifecycle of validation activities from initial planning through post-execution review and maintenance of validated status. Implement and manage execution of the company validation program: Develop and implement the validation strategy. Coordinate validation activities with relevant areas and external service providers. Oversee validation of: Infrastructure and Utilities Cleaning Equipment Software & Computer Systems (in collaboration with IT) Processes, including Shipping Test methods Author and maintain validation procedures & documents: Author and approve validation & project plans, protocols, and reports. Review qualification protocols and reports of third-party service providers. Provide technical expertise and training for validation activities: System risk assessments and required level of validation. Identification of user requirements. Project plans, protocols, and reports. Provide expertise related to relevant validation activities. Desired Experience & Qualification The following skills and experience are requirements for the position: Experience in planning and executing validation protocols - including process validation, computer systems validation, test method validation, and/or equipment qualification. Demonstrated ability to design and monitor systems using statistical methods such as Design of Experiments (DOE), Statistical Process Control (SPC), Regression Analysis, Analysis of Variance (ANOVA), and Gage Repeatability & Reproducibility (Gage R&R). ISO 13485, ISO 9001, and/or c GMP industry experience in Process Development, Quality Assurance, Quality Systems, Operations, or other related field. Broad technical knowledge of life science reagents, genomics, next-generation sequencing (NGS), PCR, and/or recombinant protein production are all highly desirable. Demonstrated scientific excellence in technical work, written communication, and presenting technical information to groups with various scientific backgrounds. The ability to multitask, perform consistently under pressure, and work without supervision. Strong interpersonal skills and an excellent ability to drive results in multi-level, cross-functional teams. Excellent organisational skills and outstanding attention to detail. Good communication and personal task management skills and a high level of self-motivation. Ability to determine project timelines and meet deadlines. Excellent written and verbal communication skills. Education and Experience An MSc in molecular biology, biochemistry or BEng Hons in Engineering or a related discipline is required. A minimum of 3 years in biotech or related industry is desirable, including positions with broad functional scope across research and development, technical transfers, manufacturing, quality control, and quality assurance. Certification or qualification as a validation engineer, such as Certified Validation Professional (CVP) or Certified Quality Validation Engineer (CQVE) is preferred. Interested? Application Procedure To apply for the position, please submit the following in PDF format on Indeed (Add Link here): Letter of motivation 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 3 references who are able to assess your suitability for the position in terms of the specified requirements will be requested. *** 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. #J-18808-Ljbffr

Product Development Technologist

Reference: CPT -GW-4

We are looking for a Product Development Technologist in the flavour, ingredient and colour industry. It is essential that you have experience in flavour formulations within the sweet division.

Duties & Responsibilities

Requirements:

• Diploma/Degree – Food Technology/Food Science
• 2-5 years’ experience with product development
• Deadline driven
• Strong verbal and written communication
• Know how to put flavour/seasoning formulations together

Duties:

• Formulate new flavours
• Flavour modification on existing products
• Develop and manipulate application formulation
• Compounding of samples
• Conducting sensory panels
• Source for new ingredients and evaluate raw materials
• Compiling of product specifications and process methods

Application Process

When applying, ensure your CV is in WORD or PDF format, and not scanned . Our software will not be able to match you to positions if it is scanned. Scanned CVs will not be considered.
Please accept your application as unsuccessful if you had no feedback within 14 days of applying. We will keep your CV on our database and match it to other suitable positions. We will contact you in the future should you match a different position.

PLEASE NOTE: We use Placement Partner to track and manage applications and can only accept applications received through this portal. We do not accept any applications by email or WhatsApp. If you are unable to apply through the link we have provided, please upload your CV to our website . We reserve the right to stop/renew adverts.

Package & Remuneration

Monthly

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Job Description

A Leading Financial Services client requires a Product Development Analyst to assist in formulating the overall strategy and design of products, features, and engagement processes.

Responsibilities

• Assist in formulating the overall strategy and design of products, features, and engagement processes.
• Conduct trend analysis within digital services.
• Take ownership of financial models used in the planning and forecasting process.
• Manage the end-to-end life cycle of products and their distribution channels, including ideation, design, and management of features.

Minimum Requirements

Matric / Grade 12

Tertiary Qualification - Bachelor's Degree or higher essential.
Minimum of 2 years of working experience in a strategy, business development, product development, management consulting, or digital services role within the Financial Services / Banking environment.
Demonstrated passion for financial technology and digital banking.

Package & Remuneration

Salary: Market Related

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