Eris Therapeutics Hiring QC, QA & ADL Officer/Executive

QC, QA & ADL Officer/Executive Openings at Eris Therapeutics

Apply now for QC, QA & ADL Officer/Executive vacancies at Eris Therapeutics. Pharma professionals with relevant qualifications and experience are invited.

URL Slug: eris-therapeutics-qc-qa-adl

Eris Therapeutics, a fast-growing pharmaceutical company, is expanding its workforce and inviting skilled professionals to join its Quality Control, Quality Assurance, and Analytical Development Laboratory (ADL) teams. This is an excellent opportunity for pharma professionals looking to advance their careers in a trusted organization that values innovation, compliance, and excellence in healthcare.

Company Overview

Eris Therapeutics is a reputed pharmaceutical company committed to delivering high-quality medicines and healthcare solutions. With a strong presence in the pharmaceutical sector, Eris has been steadily growing through its dedication to research, compliance with global regulatory standards, and focus on patient-centric solutions. The company fosters an inclusive workplace culture, offering ample growth opportunities and a supportive environment for career development.

Job Role & Responsibilities

1. QC Officer/Executive

• Conduct analysis of raw materials, intermediates, and finished formulations.
• Perform routine quality checks in compliance with GMP and regulatory standards.
• Operate analytical instruments like HPLC, GC, UV, and FTIR.
• Document results accurately and prepare reports for audits and inspections.

2. QA Officer/Executive

• Ensure compliance with cGMP, GLP, and regulatory requirements.
• Review and approve documents including SOPs, protocols, and batch records.
• Handle investigations for deviations, CAPA, and change controls.
• Conduct internal audits and support regulatory inspections.

3. ADL Officer/Executive

• Support analytical method development and validation activities.
• Work on stability studies, impurity profiling, and analytical documentation.
• Troubleshoot analytical issues and ensure compliance with regulatory guidelines.
• Prepare technical reports, validation protocols, and SOPs.

Eligibility / Qualifications

• B. Pharma / M. Pharma / M.Sc. (Chemistry or related disciplines)
• Experience range: 2–7 years (depending on role)
• Hands-on experience with pharmaceutical QC/QA/ADL processes
• Strong understanding of regulatory guidelines (USFDA, MHRA, ICH)
• Good communication and documentation skills

Location & Salary

• Location: Details will be shared upon selection.
• Salary: Competitive and based on experience.

Application Process

Interested candidates can share their updated resumes via email:

recruitment@eristherapeutics.com
9558001555, 9414100208

Apply now to secure your place in a growing and dynamic pharmaceutical organization!

Why Join Eris Therapeutics?

• Work with one of India’s fast-growing pharma companies
• Exposure to global regulatory standards
• Opportunities for career growth and continuous learning
• Competitive compensation and supportive work culture

FAQs

Q1: What is the eligibility for QC/QA/ADL roles at Eris Therapeutics?
Candidates with B. Pharma, M. Pharma, or M.Sc. qualifications and 2–7 years of experience are eligible.

Q2: What are the primary responsibilities of a QA Executive?
Ensuring compliance with GMP, reviewing documents, handling CAPA, audits, and supporting regulatory inspections.

Q3: How can I apply for these roles?
You can send your CV directly to recruitment@eristherapeutics.com with your details.

Q4: Does Eris prefer candidates with regulatory exposure?
Yes, prior experience with USFDA/MHRA/ICH guidelines will be a strong advantage.

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