Provis Biolabs, a leader in [mention your industry and specialization, e.g., peptide synthesis and analytical services], is seeking highly motivated and detail-oriented individuals to join our growing team. We offer a dynamic work environment where innovation and quality are paramount. We are currently hiring for two key positions vital to our continued success: a Quality Control (QC) Analyst and a Data & Quality Assurance (DQA) Executive. These roles offer excellent opportunities for professional growth and development within a thriving scientific organization.
Quality Control (QC) Analyst – CRO AR&D/Peptides
Experience: 1-3 years in a relevant analytical laboratory setting.
Qualifications:
- Master of Science (M.Sc.) in Chemistry, Analytical Chemistry, or Biotechnology; or Bachelor of Pharmacy (B.Pharm) / Master of Pharmacy (M.Pharm).
- Proven hands-on experience with various analytical techniques is essential.
Key Responsibilities:
This role is critical in ensuring the highest quality standards for our peptide products. The successful candidate will be responsible for:
- Performing Routine Analyses: Conducting a wide range of analytical tests, including High-Performance Liquid Chromatography (HPLC), Ultra-Performance Liquid Chromatography (UPLC), Mass Spectrometry (MS), Fourier-Transform Infrared Spectroscopy (FTIR), Ultraviolet-Visible Spectroscopy (UV), and Karl Fischer titrations on peptide samples. Precision and accuracy are paramount in this task.
- Maintaining Comprehensive Documentation: Preparing, meticulously reviewing, and maintaining all associated QC documentation, including detailed analytical reports, Certificates of Analysis (COAs), and validation protocols, ensuring complete and accurate records compliant with regulatory standards.
- Adherence to Regulatory Guidelines: Strictly following International Council for Harmonisation (ICH), Good Manufacturing Practices (GMP), and all relevant regulatory guidelines for analytical method validation and quality control processes. A thorough understanding of these regulations is essential.
- Ensuring CRO-Specific Compliance: Maintaining strict adherence to Provis Biolabs’ specific quality requirements within the context of our contract research organization (CRO) peptide synthesis projects. This includes understanding and implementing specific client requirements.
- Method Development and Validation (if applicable): Depending on experience, participation in the development and validation of new analytical methods may be required. This would involve designing experiments, executing tests, and documenting results meticulously.
Data & Quality Assurance (DQA) Executive
Experience: 1-3 years in a quality assurance or data management role within a laboratory setting.
Qualifications:
- Master of Science (M.Sc.) in Analytical Chemistry or Biotechnology; or Bachelor of Pharmacy (B.Pharm) / Master of Pharmacy (M.Pharm).
- A strong understanding of data integrity principles and GMP/GLP guidelines is required.
Key Responsibilities:
This position plays a crucial role in maintaining the integrity and accuracy of our analytical data. The successful candidate will:
- Data Integrity and Accuracy: Review and ensure the complete integrity and accuracy of all analytical results generated by HPLC, UPLC, MS, and Nuclear Magnetic Resonance (NMR) techniques. This involves thorough data review, error checking, and outlier detection.
- Good Documentation Practices (GDP): Implement and rigorously maintain Good Documentation Practices (GDP) throughout all peptide analytical workflows, ensuring compliance with internal and external standards. This includes training and guidance for laboratory staff.
- Quality Audits and Assessments: Conduct regular quality audits, comprehensive risk assessments, and thorough deviation investigations within the QC/analytical department to identify areas for improvement and prevent future issues.
- Compliance Support: Actively support laboratory audits and data compliance inspections conducted by regulatory bodies or clients, ensuring seamless and successful completion.
- SOP Development and Implementation (if applicable): Depending on experience, you might be involved in developing and implementing standard operating procedures (SOPs) to enhance laboratory efficiency and compliance.
Why Choose Provis Biolabs?
At Provis Biolabs, we are committed to fostering a collaborative and supportive work environment. We provide opportunities for continuous learning and professional development, along with a competitive compensation and benefits package. We value innovation, teamwork, and a dedication to excellence. If you are a highly motivated individual with a passion for quality and a desire to contribute to a growing company, we encourage you to apply.
Apply Now
Ready to embark on a rewarding career journey? Submit your CV and cover letter to: careers@provisbiolabs.com
