Strides Group hiring Quality Assurance

B.Pharm/M.Sc QA Openings – Strides Group Quality Assurance Hiring

Strides Group hiring QA professionals with 2–7 years experience for in-process and compliance roles. Apply now via email to join a leading pharma company.

---

Strides Group, a globally recognized pharmaceutical organization, is inviting applications from skilled professionals for Quality Assurance (QA) roles. This opportunity is ideal for candidates with hands-on experience in in-process checks, GMP compliance, and documentation within regulated manufacturing environments.

Join a company that prioritizes quality, innovation, and patient safety, and be part of a world-class team driving pharmaceutical excellence.

---

Company Overview

Strides Group is one of India’s leading pharmaceutical companies with a strong global presence across formulations, APIs, and novel drug delivery systems. Headquartered in Bengaluru, Strides operates multiple USFDA, WHO, and EU-approved facilities worldwide, supplying products to over 100 countries.

The company is committed to developing and delivering affordable, high-quality medicines that improve lives globally. Its robust manufacturing capabilities, strong regulatory track record, and focus on innovation make Strides a trusted name in the pharma industry.

---

Job Role & Responsibilities

As part of the Quality Assurance (QA) team, you will ensure product quality, regulatory compliance, and operational excellence through in-process monitoring and documentation.

Key Responsibilities:

• Perform in-process checks during production and packaging stages to ensure compliance with batch records and GMP.
• Execute and document line clearance activities at each stage of manufacturing.
• Conduct sampling at various production stages in line with defined protocols.
• Manage instrument calibration and qualification activities (DQ, IQ, OQ, PQ).
• Handle and investigate Incidents, Deviations, OOS, OOT, Change Controls, and CAPAs.
• Ensure adherence to Standard Operating Procedures (SOPs) and Good Manufacturing Practices (GMPs).
• Participate in internal audits, self-inspections, and continuous improvement initiatives.
• Collaborate with production, QC, and engineering teams to maintain compliance and efficiency.

---

Eligibility / Qualifications

Educational Qualification:

• B.Pharm, M.Pharm, or M.Sc (Chemistry, Microbiology, or related life sciences field)

Experience:

• 2–7 years of relevant experience in Quality Assurance (In-Process, Documentation, or Compliance) within a regulated pharmaceutical manufacturing environment.

Preferred Skills:

• Strong understanding of GMP, GDP, and regulatory compliance.
• Experience in sterile or solid oral dosage form manufacturing preferred.
• Good knowledge of SOP preparation, deviation management, and process validation.
• Excellent analytical, documentation, and communication skills.

Relevant Courses (comma-separated):
B.Pharm, M.Pharm Pharmaceutics, M.Sc Chemistry, GMP Training, Quality Systems Certification, Regulatory Compliance, Documentation Practices, Pharmaceutical Manufacturing Principles.

---

Location & Salary

Work Location: Strides Group Manufacturing Unit (Location as per company assignment)
Employment Type: Full-time, On-site
Experience Level: 2–7 Years
Salary: Competitive and commensurate with industry standards
Benefits: Health insurance, performance-based incentives, and professional development programs.

---

Application Process

Interested candidates who meet the eligibility criteria can share their updated resumes via email.

Email: anupama.kv@arcolab.com

Subject Line: Application – QA Department – [Your Name]

Documents to Include:

• Updated Resume
• Educational and Experience Certificates
• Latest Salary Slip / CTC Details

Note: Candidates with experience in USFDA, MHRA, or WHO-audited plants will be given preference.

---

Why Join Strides Group?

• Work with a USFDA-approved, globally recognized pharmaceutical organization.
• Gain exposure to diverse dosage forms and regulatory frameworks.
• Opportunity to contribute to quality systems excellence and continuous improvement projects.
• Competitive compensation with strong career growth prospects.
• Collaborative work environment promoting learning, safety, and innovation.

---

FAQs

Q1. What is the required qualification for the QA role?
A1. Candidates should hold a B.Pharm, M.Pharm, or M.Sc in Chemistry, Microbiology, or a related field.

Q2. How many years of experience are needed?
A2. Applicants must have 2–7 years of experience in Quality Assurance within a pharmaceutical manufacturing unit.

Q3. What kind of QA functions are involved?
A3. The role covers in-process checks, line clearance, deviation handling, calibration, and documentation compliance.

Q4. Is experience in sterile manufacturing mandatory?
A4. It’s not mandatory but preferred, especially for candidates from regulated environments.

Q5. How can candidates apply?
A5. Email your updated resume to anupama.kv@arcolab.com with the subject line mentioning your role and experience.

---

Company	Strides Group
Vacancies	Quality Assurance (In-Process, Documentation, Compliance)
Required Education	B.Pharm / M.Pharm / M.Sc (Chemistry, Microbiology)
Experience	2–7 Years (Pharma Manufacturing QA)
Location	As per Strides Group Unit Assignment