Title: Officer, Quality Department (Quality Assurance)
Company Name: Nuvista Pharma Limited
Vacancy: --
Location: Gazipur (Tongi)
Salary: Negotiable
Experience:
∎ At most 3 years
∎ The applicants should have experience in the following business area(s):Pharmaceutical/Medicine Companies
∎ Freshers are also encouraged to apply.
Published: 8 Apr 2024
Education:
∎ M.Pharm/ B.Pharm (5 Years Professional Degree) from any reputed University.
∎ M.Pharm/ B.Pharm (5 Years Professional Degree) from any reputed University.
Requirements:
Additional Requirements:
∎ Extensively demonstrated pharmaceutical quality experience, including the development and management of quality systems such as audit programs, change control, complaint handling and investigations experience.
∎ A thorough knowledge of pharmaceutical internal/external manufacturing, packaging, testing, and distribution processes and associated global regulatory GMP/GDP requirements.
∎ Experience of supporting regulatory inspections, client audits and self-inspections.
∎ Solid understanding of the requirements of an effective Pharmaceuticals Quality System.
∎ Computer Literacy
∎ Strong Communication Skill.
∎ Extensively demonstrated pharmaceutical quality experience, including the development and management of quality systems such as audit programs, change control, complaint handling and investigations experience.
∎ A thorough knowledge of pharmaceutical internal/external manufacturing, packaging, testing, and distribution processes and associated global regulatory GMP/GDP requirements.
∎ Experience of supporting regulatory inspections, client audits and self-inspections.
∎ Solid understanding of the requirements of an effective Pharmaceuticals Quality System.
∎ Computer Literacy
∎ Strong Communication Skill.
Responsibilities & Context:
∎ Write, review, implement and maintain a Quality Management System (i.e Deviation, Investigation, risk assessment, change control, CAPA, customer complaint, recall etc.
∎ In-process testing/inspection, line clearance & sampling of products (Intermediate & Finished products).
∎ Batch document compilation, release follow-up & archiving.
∎ Perform Annual Product Quality Review (APQR) of finished products.
∎ Job Responsibilities:
∎ Write, review, implement and maintain a Quality Management System (i.e Deviation, Investigation, risk assessment, change control, CAPA, customer complaint, recall etc.
∎ In-process testing/inspection, line clearance & sampling of products (Intermediate & Finished products).
∎ Batch document compilation, release follow-up & archiving.
∎ Perform Annual Product Quality Review (APQR) of finished products.
Employment Status: Full Time
Job Location: Gazipur (Tongi)
Read Before Apply:
If you believe that you are the right person for the winning team, apply online or email your resume to : [email protected] with the position applied for clearly mentioned in the subject line by
Only short listed candidates will be invited for further selection process Nuvista Pharma Limited is an equal opportunities employer. Candidates of any gender, race, ethnicity are highly encouraged to apply.
Source: bdjobs.com