Global QA Specialist - Computerized Systems at PolyPeptide US

Ambernath, maharashtra, India -

Full Time

Start Date

Immediate

Expiry Date

28 Jan, 26

Salary

0.0

Posted On

30 Oct, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Quality Assurance, Computerized Systems, GMP Compliance, Validation, Digitalization Projects, Audits, Risk Assessments, Documentation, Communication Skills, Scientific Life Sciences, ERP Systems, LIMS Systems, Change Requests, Deviations, Software Qualification, Regulatory Requirements

Industry

Pharmaceutical Manufacturing

Description

Job Title: Global QA Specialist Location: Ambernath, India Job Type: Full Time Reporting: Global QA Senior Specialist, Global Quality Assurance About PolyPeptide Group: PolyPeptide Group AG and its consolidated subsidiaries (“PolyPeptide”) is a specialized Contract Development & Manufacturing Organization (CDMO) for peptide- and oligonucleotide-based active pharmaceutical ingredients. By supporting its customers mainly in pharma and biotech, it contributes to the health of millions of patients across the world. PolyPeptide serves a fast-growing market, offering products and services from pre-clinical to commercial stages. Its broad portfolio reflects the opportunities in drug therapies across areas and with a large exposure to metabolic diseases, including GLP-1. Dating back to 1952, PolyPeptide today runs a global network of six GMP-certified facilities in Europe, the U.S. and India. PolyPeptide’s shares (SIX: PPGN) are listed on SIX Swiss Exchange. Position Overview: We’re looking for a passionate and experienced professional to join our Global QA team. As a global QA specialist working with global computerized systems, you will have an operational focus when being involved in many parts of our business and need to navigate in an environment that has a high tempo and is changeable to able to meet the high demands. Key Responsibilities: Actively support digitalization projects. Actively support validation of GMP related computerized systems Support preparation of life cycle documentation for GMP related computerized systems, e.g., validation documents, periodic reviews, change requests, deviations, risk assessments, procedures Support in audits by authorities and customers of PolyPeptide Support in qualification of software vendors Must-Have Qualifications: We believe that you are ready for new and exciting challenges in a global QA role. You have several years of experience with QA work and validation of computerized systems within the pharma or medical device industry. You have high GMP understanding as well as knowledge of regulatory requirements, and guidelines related to computerized systems and GMP compliance (e.g., 21 CFR Part 11, Data integrity, GAMP 5). You enjoy supporting and coach co-workers but are also able to challenge procedures and introduce alternative options. You need to have: Minimum 5 years’ experience within Pharma or Medical Device industry Minimum 3 years’ experience within a quality function Excellent communications skills in English Bachelor/Master/PhD degree in scientific life sciences, or equal Auditor qualification is a merit Describe in the application: Which QMS, ERP, LIMS systems you have worked in and in which roles. Which types of documents you have worked with, for which type of systems (QMS, ERP, LIMS, equipment/instrument software) and in which roles (author, reviewer, approver). Why Join Us at PolyPeptide Group: PolyPeptide Group offers an exciting opportunity to work at the forefront of peptide-based therapeutics, a rapidly growing and innovative segment of the pharmaceutical industry. As a key member of PolyPeptide team, you will have the opportunity to contribute to a company that is dedicated to the success of its clients and the advancement of peptide science. Join us and be part of a global organization that is shaping the future of life-saving therapies.

Responsibilities

The Global QA Specialist will actively support digitalization projects and the validation of GMP-related computerized systems. They will also assist in preparing life cycle documentation and support audits by authorities and customers.