Sr. Officer (PV) Jobs in Acme Generics LLP - Baddi, Himachal Pradesh

Sr. Officer (PV) Jobs in Acme Generics LLP - Baddi, Himachal Pradesh

work outline icon2 - 9 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

Acme Generics LLP

time outline iconBaddi, Himachal Pradesh, India

Posted on 24-02-2026

1 Vacancy

Description

Job Requirements

  1. Job Title: Sr. Officer-QC (PV)
  2. Location: Indira Acme Generics LLP - Baddi, Himachal Pradesh
  3. Qualification: BPharm
  4. Work Experience: 2 to 9 Years

Job Description

  1. Oversee and manage pharmacovigilance activities, including adverse event (AE) and serious adverse event (SAE) reporting.
  2. Review, evaluate, and validate safety data from clinical trials, post-marketing surveillance, and literature.
  3. Ensure timely submission of safety reports (SUSARs, PSURs, DSURs) to regulatory authorities.
  4. Monitor compliance with global PV regulations, ICH guidelines, and company SOPs.
  5. Coordinate with clinical, regulatory, and medical teams for safety queries and data reconciliation.

Take this opportunity to join Indira Acme Generics LLP - Baddi, as an Sr. Officer-QC (PV) in Baddi, Himachal Pradesh, and build a successful career in the healthcare industry. Apply today for this job opportunity and grow with a leading healthcare organization.

Category

Pharmaceuticals

Preferred Education

BPharm (Bachelor Of Pharmacy)

Key Skills

Communication SkillsDecision MakingSelf-motivationLeadership

About Organization

Acme Generics is a pharmaceutical manufacturing company that operates within the broader Acme Group, providing contract manufacturing, research, and development services to leading Indian and global pharmaceutical companies. Headquarters / Facility: Plot No. 115, HPSIDC Industrial Area, Davni, P.O. Gurumajra, Tehsil Nalagarh, District Solan, Himachal Pradesh – 174101, India. The core focus is on pharmaceutical contract manufacturing of oral solid dosage forms (tablets, capsules) and sterile products. It also offers finished product development, regulatory filings, R&D services, and licensing support to global pharmaceutical partners, emphasizing quality, compliance, and innovation.

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