Job Opportunity: Dynamic Pharma Professionals Needed for Expansion Units
Summary: We are seeking dedicated and experienced pharmaceutical professionals to join our rapidly growing manufacturing facilities at Stanford Laboratories (Mehatpur, HP) and Larenon Healthcare (Ghiloth, Rajasthan). We are hiring across Quality Assurance, Quality Control, F&D, and ADL departments for candidates with 1–5 years of relevant experience in OSD (Oral Solid Dosage) manufacturing. This is an excellent opportunity for professionals looking to build a career in a high-compliance, growth-oriented environment.
About the Opportunity
As part of our strategic business expansion, we are scaling our operations at two of our premier manufacturing units:
- Stanford Laboratories: Located in Mehatpur, Himachal Pradesh.
- Larenon Healthcare: Located in the industrial hub of Ghiloth, Neemrana, Rajasthan.
We are looking for passionate, result-oriented individuals who are eager to contribute to a culture of excellence, innovation, and strict regulatory compliance. Whether you are an experienced professional looking for a new challenge or a specialist in pharmaceutical manufacturing, these roles offer a clear path for professional development and exposure to large-scale, modern manufacturing processes.
Open Positions
We are currently inviting applications for the following critical roles:
- Quality Assurance (QA): Multiple openings for our units in both UNA (Mehatpur) and Ghiloth.
- Quality Control (QC): Multiple openings for our units in both UNA (Mehatpur) and Ghiloth.
- Formulation & Development (F&D): Openings specifically for our UNA location.
- Analytical Development Lab (ADL): Openings specifically for our UNA location.
Eligibility Criteria
To be considered for these positions, candidates must meet the following requirements:
- Academic Background: B. Pharma or M. Pharma is required for all QA and R&D roles. An M. Sc. degree is required for QC positions.
- Experience: A minimum of 1 to 5 years of relevant experience within a pharma manufacturing environment is mandatory.
- Specialization: Candidates must have solid experience in OSD (Oral Solid Dosage) manufacturing.
- Preferred Skills: Candidates with previous exposure to regulated plants, meticulous documentation practices, and active participation in regulatory audits will be given priority.
Key Skills & Responsibilities
Selected candidates will be expected to uphold our high standards of excellence. You should possess:
- In-depth knowledge of cGMP (current Good Manufacturing Practice) and GLP (Good Laboratory Practice).
- Proven expertise in maintaining high-quality documentation standards.
- Experience handling regulatory compliance, internal and external audits, and process validations.
- Strong analytical and problem-solving skills to navigate complex manufacturing challenges.
- The adaptability to thrive in a fast-paced, high-capacity production environment.
Why Choose a Career with Us?
- Professional Growth: Work with rapidly expanding organizations that value internal talent and offer clear career advancement paths.
- Cutting-Edge Exposure: Gain hands-on experience in greenfield and high-capacity plants equipped with the latest technology.
- Cultivating Excellence: Join a team that prioritizes a learning-driven culture, innovation, and adherence to global quality standards.
- Stability: Become part of a stable, compliance-focused work environment that invests in the long-term success of its employees.
How to Apply
If you are ready to take the next step in your pharmaceutical career, we encourage you to reach out. Please submit your updated CV, highlighting your relevant experience in OSD manufacturing, to the contact details provided below:
- Email: Send your resume to [email protected]
- Contact Number: For any specific queries, feel free to reach out to us at +91 9810846443.
We look forward to reviewing your application and discussing how your skills and expertise can contribute to our continued success in the pharmaceutical industry.