Cubit Lifesciences LLP has announced new recruitment opportunities for experienced pharmaceutical professionals in the Formulation Manufacturing industry. The company is inviting applications for Production & Packing Officer/Executive and Quality Control Officer positions. Candidates with B.Pharm, M.Pharm, B.Sc, or M.Sc qualifications and relevant pharmaceutical formulation experience are encouraged to apply.

If you are looking for a stable career in a growing pharmaceutical organization, this is an excellent opportunity to join Cubit Lifesciences LLP.

Organization Details

Company Name: Cubit Lifesciences LLP

Industry: Pharmaceutical Formulation Manufacturing

Job Type: Full-Time

Location: As per company requirements

Selection Process: Shortlisting followed by Interview

Available Job Openings

1. Production & Packing – Officer / Executive

Qualification:

B.Pharm

M.Pharm

B.Sc

M.Sc

Experience:

1–5 Years

Industry:

Pharmaceutical Formulation

2. Quality Control (QC) – Officer

Qualification:

B.Pharm

M.Pharm

B.Sc

M.Sc

Experience:

1–3 Years

Industry:

Pharmaceutical Formulation

Educational Qualification

Candidates must possess any of the following qualifications:

B.Pharm

M.Pharm

B.Sc

M.Sc

Experience Required

Production & Packing: 1 to 5 years

Quality Control: 1 to 3 years

Relevant experience in pharmaceutical formulation manufacturing is preferred.

Application Process

Interested and eligible candidates should send their updated CV to:

Email: hr@cubitgroup.in

WhatsApp: 7859800724

Information to Mention in Your Application

Candidates should include the following details in their CV or email:

Total Years of Experience

Current CTC

Expected CTC

Notice Period

Preferred Date for Face-to-Face Interview

Why Join Cubit Lifesciences LLP?

Opportunity to work with a rapidly growing pharmaceutical company

Professional learning and career development

Dynamic and collaborative work environment

Quality-driven and ethical manufacturing practices

Long-term career growth opportunities

Selection Process

Application Screening

Shortlisting of Eligible Candidates

Face-to-Face Interview

Final Selection

Offer Letter and Joining

Only shortlisted candidates will be contacted for the next stage of the recruitment process.

Important Highlights

Hiring for Production & Packing and Quality Control departments

Pharmaceutical Formulation Industry

B.Pharm, M.Pharm, B.Sc & M.Sc candidates can apply

Relevant experience is mandatory

Applications accepted via Email and WhatsApp

Excellent opportunity for experienced pharma professionals

Technical FAQs

1. What responsibilities does a Production & Packing Officer perform in a pharmaceutical formulation plant?

A Production & Packing Officer oversees manufacturing operations, line clearance, batch documentation, equipment operation, GMP compliance, packaging activities, productivity improvement, and ensures products meet quality and regulatory standards.

2. What analytical instruments should a Quality Control Officer be familiar with?

A QC Officer should have knowledge of analytical instruments such as HPLC, UV-Visible Spectrophotometer, Dissolution Apparatus, FTIR, pH Meter, Karl Fischer Titrator, GC (where applicable), and stability testing procedures.

3. Why is GMP important in pharmaceutical manufacturing?

Good Manufacturing Practices (GMP) ensure medicines are consistently produced and controlled according to quality standards, minimizing contamination, documentation errors, product mix-ups, and regulatory non-compliance.

4. What documents are commonly maintained in pharmaceutical production and quality departments?

Common documents include Batch Manufacturing Records (BMR), Batch Packaging Records (BPR), Standard Operating Procedures (SOPs), Equipment Logbooks, Calibration Records, Cleaning Records, Change Controls, Deviations, CAPA, and Validation documents.

5. Which regulatory guidelines are commonly followed in pharmaceutical formulation manufacturing?

Pharmaceutical companies generally follow WHO-GMP, Schedule M, ICH Guidelines, Good Documentation Practices (GDP), Data Integrity principles (ALCOA+), and other applicable national and international regulatory requirements.