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SynThera Biomedical
Job Description
Job Advertisement – Quality Assurance (QA) & Quality Control (QC) Associate
Location: Vasai, Maharashtra
About SynThera Biomedical Pvt. Ltd.
SynThera Biomedical Pvt. Ltd. is an advanced materials company focused on the research, development, manufacturing, and commercialization of specialty glass and advanced material products for high-technology applications. The Company's core expertise is in bioactive glass, with applications across healthcare, oral care, medical devices, cosmetics, and other emerging sectors.
SynThera has developed multiple products and technologies that are among the first of their kind in India, with several representing globally novel innovations. The Company's technology portfolio includes multiple patents granted and filed in India and internationally, as well as peer-reviewed scientific publications.
SynThera has established India's first commercial manufacturing facility for bioactive glass and is working to scale its technologies from laboratory development through pilot production to commercial manufacturing. The Company works with customers, research institutions, manufacturing partners, laboratories, and other organizations in India and internationally.
Joining SynThera offers an opportunity to work in a hands-on, technology-driven environment with considerable exposure to advanced manufacturing, product development, commercialization, and cross-functional learning.
Job Summary
As a Quality Assurance (QA) & Quality Control (QC) Associate, you will play a key role in ensuring that the Company's raw materials, processes, and finished products consistently meet established quality standards and applicable regulatory requirements.
You will work closely with R&D;, Production, Supply Chain, external laboratories, vendors, and other stakeholders on quality systems, analytical testing, documentation, validation, investigations, audits, and continuous improvement.
The role is particularly suited to science and pharmacy graduates interested in developing practical experience in pharmaceutical, healthcare, and advanced-material quality systems, analytical testing, documentation, and regulatory compliance.
Key Responsibilities
Perform routine quality control testing of raw materials, in-process samples, finished products, and packaging materials.
Conduct analytical, chemical, microbiological, and physical testing using established test methods and SOPs.
Maintain accurate laboratory records, analytical reports, and documentation in accordance with Good Documentation Practices (GDP).
Support compliance with applicable cGMP, Quality Management Systems (QMS), and regulatory requirements.
Prepare, review, and maintain SOPs, specifications, test methods, protocols, and quality records.
Participate in investigations relating to out-of-specification (OOS), out-of-trend (OOT), deviations, non-conformances, customer complaints, and corrective and preventive actions (CAPA).
Support equipment qualification, process validation, cleaning validation, and analytical method validation activities.
Coordinate calibration, preventive maintenance, and qualification of laboratory instruments and equipment.
Assist in vendor qualification, supplier quality evaluations, incoming material inspections, and quality audits.
regulatory inspections.
Monitor environmental and laboratory quality parameters as applicable.
Assist in product stability studies and compilation and analysis of quality data.
Coordinate with external laboratories for analytical testing and documentation.
Support preparation of technical documents, product dossiers, regulatory submissions, certificates, and quality-related reports.
Participate in continuous improvement initiatives to strengthen product quality, laboratory efficiency, documentation, and compliance.
Perform other QA/QC responsibilities assigned from time to time.
Candidate Profile
Educational Qualification
B.Pharm / M.Pharm / D.Pharm; or
B.Sc. / M.Sc. in Chemistry, Microbiology, Biotechnology, Biochemistry, or another relevant discipline.
Final-year students pursuing B.Pharm, M.Pharm, B.Sc., or M.Sc. may also apply.
Experience
Freshers and recent graduates are encouraged to apply.
Candidates with 0–2 years of relevant experience in QA, QC, analytical laboratories, pharmaceuticals, healthcare, chemicals, materials, or related sectors will also be considered.
Desired Skills
Basic understanding of GMP, GLP, GDP, and pharmaceutical quality systems.
Knowledge of analytical laboratory techniques and quality testing.
Strong documentation, data-analysis, and report-writing skills.
Strong attention to detail and a quality-focused mindset.
Ability to identify problems, investigate root causes, and recommend corrective actions.
Be able to join immediately or within a short notice period.
Be comfortable working in a laboratory and manufacturing environment.
Be willing to travel for Company-related activities when required.
Candidates from Vasai–Virar, Palghar, Mira Road, Bhayandar, and nearby areas will be preferred.
Candidates applying from outside the region will be responsible for their own accommodation and travel arrangements.
Application
Interested candidates should send their CV via WhatsApp to +91 97309 99356 .
Shortlisted/eligible applicants will be sent an application form to provide additional information required for the recruitment process.
Alternatively, candidates may email their CV to .
SynThera Biomedical Private Limited
CIN: U33111PN2015PTC155498
GSTIN: 27AAVCS9466L1Z4
Postal Address:
Building No. 7, Gala No. 05,
Nirav Industrial Estate, Sativali,
Vasai (East), Maharashtra – 401208
Registered Office:
E-202, Felicita, Baner-Pashan Link Road,
Baner, Pune – 411045, India
Tel: +91 97309 99356
Website: www.synthera.in
Email:
Location: Vasai, Maharashtra
About SynThera Biomedical Pvt. Ltd.
SynThera Biomedical Pvt. Ltd. is an advanced materials company focused on the research, development, manufacturing, and commercialization of specialty glass and advanced material products for high-technology applications. The Company's core expertise is in bioactive glass, with applications across healthcare, oral care, medical devices, cosmetics, and other emerging sectors.
SynThera has developed multiple products and technologies that are among the first of their kind in India, with several representing globally novel innovations. The Company's technology portfolio includes multiple patents granted and filed in India and internationally, as well as peer-reviewed scientific publications.
SynThera has established India's first commercial manufacturing facility for bioactive glass and is working to scale its technologies from laboratory development through pilot production to commercial manufacturing. The Company works with customers, research institutions, manufacturing partners, laboratories, and other organizations in India and internationally.
Joining SynThera offers an opportunity to work in a hands-on, technology-driven environment with considerable exposure to advanced manufacturing, product development, commercialization, and cross-functional learning.
Job Summary
As a Quality Assurance (QA) & Quality Control (QC) Associate, you will play a key role in ensuring that the Company's raw materials, processes, and finished products consistently meet established quality standards and applicable regulatory requirements.
You will work closely with R&D;, Production, Supply Chain, external laboratories, vendors, and other stakeholders on quality systems, analytical testing, documentation, validation, investigations, audits, and continuous improvement.
The role is particularly suited to science and pharmacy graduates interested in developing practical experience in pharmaceutical, healthcare, and advanced-material quality systems, analytical testing, documentation, and regulatory compliance.
Key Responsibilities
Perform routine quality control testing of raw materials, in-process samples, finished products, and packaging materials.
Conduct analytical, chemical, microbiological, and physical testing using established test methods and SOPs.
Maintain accurate laboratory records, analytical reports, and documentation in accordance with Good Documentation Practices (GDP).
Support compliance with applicable cGMP, Quality Management Systems (QMS), and regulatory requirements.
Prepare, review, and maintain SOPs, specifications, test methods, protocols, and quality records.
Participate in investigations relating to out-of-specification (OOS), out-of-trend (OOT), deviations, non-conformances, customer complaints, and corrective and preventive actions (CAPA).
Support equipment qualification, process validation, cleaning validation, and analytical method validation activities.
Coordinate calibration, preventive maintenance, and qualification of laboratory instruments and equipment.
Assist in vendor qualification, supplier quality evaluations, incoming material inspections, and quality audits.
regulatory inspections.
Monitor environmental and laboratory quality parameters as applicable.
Assist in product stability studies and compilation and analysis of quality data.
Coordinate with external laboratories for analytical testing and documentation.
Support preparation of technical documents, product dossiers, regulatory submissions, certificates, and quality-related reports.
Participate in continuous improvement initiatives to strengthen product quality, laboratory efficiency, documentation, and compliance.
Perform other QA/QC responsibilities assigned from time to time.
Candidate Profile
Educational Qualification
B.Pharm / M.Pharm / D.Pharm; or
B.Sc. / M.Sc. in Chemistry, Microbiology, Biotechnology, Biochemistry, or another relevant discipline.
Final-year students pursuing B.Pharm, M.Pharm, B.Sc., or M.Sc. may also apply.
Experience
Freshers and recent graduates are encouraged to apply.
Candidates with 0–2 years of relevant experience in QA, QC, analytical laboratories, pharmaceuticals, healthcare, chemicals, materials, or related sectors will also be considered.
Desired Skills
Basic understanding of GMP, GLP, GDP, and pharmaceutical quality systems.
Knowledge of analytical laboratory techniques and quality testing.
Strong documentation, data-analysis, and report-writing skills.
Strong attention to detail and a quality-focused mindset.
Ability to identify problems, investigate root causes, and recommend corrective actions.
Be able to join immediately or within a short notice period.
Be comfortable working in a laboratory and manufacturing environment.
Be willing to travel for Company-related activities when required.
Candidates from Vasai–Virar, Palghar, Mira Road, Bhayandar, and nearby areas will be preferred.
Candidates applying from outside the region will be responsible for their own accommodation and travel arrangements.
Application
Interested candidates should send their CV via WhatsApp to +91 97309 99356 .
Shortlisted/eligible applicants will be sent an application form to provide additional information required for the recruitment process.
Alternatively, candidates may email their CV to .
SynThera Biomedical Private Limited
CIN: U33111PN2015PTC155498
GSTIN: 27AAVCS9466L1Z4
Postal Address:
Building No. 7, Gala No. 05,
Nirav Industrial Estate, Sativali,
Vasai (East), Maharashtra – 401208
Registered Office:
E-202, Felicita, Baner-Pashan Link Road,
Baner, Pune – 411045, India
Tel: +91 97309 99356
Website: www.synthera.in
Email:
