Hiring.Camp

Sr. Manager / DGM – Quality Assurance & Quality Control

Scimplify

·

Sep 16, 2026

Location
Vadodara, India · Bangalore, India
Department
Manufacturing
Seniority
Manager
Education
Master
Source
Keka

Description

About Scimplify

Scimplify is a specialty chemicals manufacturing company offering a full-stack solution—from R&D and custom synthesis to large-scale manufacturing and doorstep delivery. Headquartered in Bengaluru, India, we serve multiple industries ranging from pharmaceuticals to agrochemicals and industrial chemicals to personal care and fragrances.

We enable 1000+ business across 30+ countries to develop and scale innovative chemicals from lab to commercial production.We have raised $40 million in Series B funding, taking its total funding to $54 million. The round was co-led by Accel and Bertelsmann India Investments.We are a team of 450+ professionals with entities in India, Japan, USA, UAE, and Indonesia.


Job Summary:
Lead the overall QA & QC function for pharmaceutical and specialty chemical products, ensuring compliance with GMP, QMS, regulatory requirements and customer specifications.

Key Responsibilities:

  • Lead QA & QC operations, QMS, SOPs, deviations, OOS/OOT, CAPA and change controls.
  • Manage QC laboratory activities, analytical testing, method development, validation and transfer.
  • Ensure quality compliance for raw materials, intermediates and finished products.
  • Lead vendor/CMO qualification, audits and supplier quality management.
  • Handle customer complaints, quality queries, specifications and customer audits.
  • Coordinate regulatory, internal and external audits and ensure timely CAPA closure.
  • Drive quality risk management, data integrity and continuous improvement.
  • Develop and manage QA/QC team, KPIs, budgets and laboratory capabilities.
  • Support new product development, product qualification and business expansion.

Qualification:
M.Sc. / M.Pharm / B.Pharm / relevant technical qualification.

Experience:
10–15 years for Senior Manager / 15–20+ years for DGM in Pharma, API, Specialty Chemicals or related industries.

Preferred:
Strong experience in GMP/QMS, analytical QC, method validation, vendor/CMO audits, customer audits, investigations and team leadership.

Skills

GMPRisk ManagementCompliance

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