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Avenza Pharmaceuticals Pvt Ltd, a reputed name in the pharmaceutical industry, is expanding its Quality Control team and is actively seeking young and dynamic professionals with a strong background in Pharmaceuticals (OSD Formulation). The company is particularly interested in candidates with proven experience in regulated markets such as USFDA, MHRA, TGA, and EU-GMP.
As the pharmaceutical industry continues to grow and evolve, the demand for highly skilled professionals specializing in quality control is increasing. Avenza Pharmaceuticals is committed to upholding the highest standards of quality, precision, and compliance, and they are looking for talented individuals to join their expanding team in Vadodara.
Open Positions and Requirements
Avenza Pharmaceuticals has announced multiple openings in the Quality Control (QC) division, targeting experienced professionals for the following roles:
GLP Specialist (4-8 years experience | Male only)
Responsibilities include SOP preparation, instrument qualification, and standard management.
HPLC Open Lab Expert (4-7 years experience | Male only)
Candidates should have expertise in chromatography, deep knowledge of open lab operations, audit trail review, reporting template creation, and processing & calculation of chromatograms.
QMS Specialist (5-8 years experience)
The role involves handling Change Control, Deviation, CAPA & Investigations, along with impact and risk assessments.
QC Investigation Analyst (4-6 years experience | Male only)
Professionals will handle Out-of-Specification (OOS), Out-of-Trend (OOT), and Pharma Out-of-Compliance (OOC) investigations and report preparation.
RM/PM Analyst (2-3 years experience | Male only)
This position focuses on excipient and API analysis according to EP/BP/USP/IP standards.
Why Join Avenza Pharmaceuticals?
Avenza Pharmaceuticals is known for its dedication to quality, innovation, and teamwork. Working in a regulated market environment, the company offers professionals an opportunity to advance their careers while contributing to the development of high-quality pharmaceutical products that meet global standards.
The company prefers immediate joiners and offers a dynamic work environment based in Vadodara.
How to Apply
Interested candidates are encouraged to send their updated resumes to seema@avenzapharma.com
with the subject line indicating the position they are applying for (e.g., Application for QC-GLP/QMS/etc.).
Avenza Pharmaceuticals Pvt Ltd invites qualified professionals to be part of their journey towards excellence in pharmaceutical quality control and compliance. If you have the expertise and passion for maintaining the highest standards, this is your chance to join a growing team in a thriving industry.
