Vital Syntheticlabs Pvt Ltd, a leading manufacturer of pyridine derivatives, speciality chemicals, APIs, and intermediates, is actively expanding its team at its API manufacturing facility in Pashamylaram, Hyderabad, Telangana. The company, known for its commitment to quality and innovation in the pharmaceutical sector, is inviting motivated and dedicated professionals to join its operations.

This is an excellent opportunity for experienced candidates in quality control, quality assurance, and research & development to contribute to a dynamic environment focused on producing high-quality pharmaceutical intermediates and speciality products.

Open Positions and Experience Requirements

Vital Syntheticlabs is seeking skilled professionals for the following roles:

• Quality Control (QC): Candidates with 2-5 years of experience in QC activities, including testing, analysis, and documentation in API/pharma manufacturing.
• Quality Assurance (QA): Professionals with 2-4 years of experience in QA functions such as compliance, audits, documentation, and ensuring GMP standards.
• Research & Development (R&D): Individuals with 2-5 years of experience in R&D, process development, or synthesis related to pyridine derivatives or speciality chemicals.

Important Note: Only male candidates are eligible to apply for these positions.

Key Details for Application

• Interview Date: Sunday, February 8, 2026
• Time: 9:00 AM to 2:00 PM
• Interview Venue: Pharma Jobs Talent Acquisition Center, Near IDPL Degree College, 2nd Floor, Bhagayarathi Talent Acquisition Center, Near IDPL X Road, Chinthal Road, Hyderabad
• Job Location: Vital Syntheticlabs Pvt Ltd, 2nd Floor, Plot No. 278 Part, Phase 1, Pashamylaram, Hyderabad, Telangana 502307
• Contact: Call 75659426391 for any queries

Candidates are encouraged to attend the walk-in interview with updated resumes, educational certificates, experience letters, and recent passport-size photographs.

Roles and Responsibilities (General for These Positions)

In these roles at Vital Syntheticlabs, selected candidates will be responsible for:

• Conducting analytical testing and ensuring product quality meets regulatory standards (for QC).
• Overseeing compliance, documentation, and quality systems in line with GMP and other pharma guidelines (for QA).
• Supporting process optimization, new molecule development, and scale-up activities (for R&D).
• Collaborating with cross-functional teams to maintain high standards of safety, quality, and efficiency in API manufacturing.

Required Qualifications and Skills

• Educational background: Typically B.Sc./M.Sc. in Chemistry, B.Pharm/M.Pharm, or related fields (based on pharma industry norms for these roles).
• Hands-on experience in API manufacturing, instrumentation (HPLC, GC, etc.), and regulatory compliance.
• Strong attention to detail, problem-solving abilities, and teamwork.
• Knowledge of GMP, ICH guidelines, and pharma documentation practices.

Salary and Benefits

While specific salary details are not disclosed in the announcement, similar positions in Hyderabad’s API manufacturing sector for candidates with 2-5 years of experience typically range from ₹3.5 LPA to ₹6.5 LPA, depending on qualifications, skills, and negotiation. The company offers a competitive compensation package, including statutory benefits, professional growth opportunities, and a supportive work environment in the pharmaceutical industry.

How to Apply

Interested and eligible candidates should attend the walk-in interview on February 8, 2026, at the specified venue. No prior registration is required—just bring all necessary documents. For directions or clarifications, contact the provided number: 75659426391.

Don’t miss this chance to join a reputed player in the speciality chemicals and API space. Prepare your profile and head to the interview venue!