Pharma / Facility Executive / OSD Packaging / QMS Production/HVAC

Job Title: HVAC Executive (MNC)

Industry: Pharmaceutical

Location: Bari Brahmana (Jammu)

Experience Required: Minimum 5 Years

Salary: Up to 7 LPA

9796871050

Job Description:

We are looking for an experienced HVAC Executive to join our team in the pharmaceutical industry. The ideal candidate should have hands-on experience in HVAC system validation, operation, and maintenance along with a strong understanding of Quality Management Systems (QMS).

Key Responsibilities:

Ensure smooth operation, preventive maintenance, and breakdown maintenance of HVAC systems.

Execute and monitor validation activities for HVAC systems as per regulatory guidelines.

Maintain proper documentation in compliance with cGMP, regulatory, and company requirements.

Prepare and review SOPs related to HVAC operations and maintenance.

Coordinate with cross-functional teams to ensure uninterrupted facility operations.

Support quality audits and inspections by providing HVAC-related documents and compliance reports.

Monitor and control environmental conditions (temperature, humidity, differential pressure, etc.).

Implement energy efficiency and cost optimization measures in HVAC operations.

Ensure adherence to QMS standards including deviation handling, CAPA, and change control.

Desired Candidate Profile:

B.Tech in Mechanical related engineering discipline.

Minimum 5 years of experience in HVAC operations and maintenance in a pharmaceutical manufacturing environment.

Strong knowledge of HVAC validation, QMS practices, and regulatory compliance.

Ability to troubleshoot HVAC equipment and systems.

Excellent documentation, analytical, and communication skills.

https://www.linkedin.com/in/satnam-singh-37b9b518/

Job Title: Facility Management & Administration Executive / Sr. Executive

Industry: Pharmaceutical

Location: Bari Brahmana (Jammu)

Experience Required: 5+ Years (in Pharma Industry)

Salary: Up to 7 LPA (Negotiable)

9796871050

Job Description:

We are looking for an experienced Facility Management & Administration Executive/Sr. Executive with strong exposure to pharmaceutical industry facility operations. The candidate will be responsible for managing housekeeping, pest control, laundry, security, canteen services, contract labour management, and ensuring compliance with QMS and cGMP requirements.

Key Responsibilities:

Oversee facility management services including housekeeping, pest control, laundry, security, and canteen operations.

Manage and monitor contract labour workforce ensuring compliance with labour laws and company policies.

Implement and monitor QMS practices in facility operations with adherence to pharma industry standards.

Coordinate with internal departments to ensure seamless support for production and administrative functions.

Ensure compliance with cGMP, safety standards, and regulatory requirements in all facility-related operations.

Prepare and maintain records, SOPs, and documentation related to facility management.

Handle vendor management, service contracts, and negotiations.

Support audits and inspections by providing facility and administration compliance documents.

Drive continuous improvement initiatives in facility management and cost optimization.

Desired Candidate Profile:

Graduate / Diploma / MBA preferred with relevant specialization.

5+ years of experience in facility management & administration in a pharmaceutical industry.

Strong knowledge of QMS, cGMP, and pharma compliance requirements.

Experience in managing contract labour and third-party vendors.

Excellent organizational, leadership, and communication skills.

https://www.linkedin.com/in/satnam-singh-37b9b518/

Job Title: QMS Production Executive

Industry: Pharmaceutical (OSD Plant)

Location: Bari Brahmana (Jammu)

Experience Required: 5+ Years (OSD Pharma Plant)

Salary: Around 6 LPA

9796871050

Job Description:

We are seeking an experienced QMS Production Executive to join our Oral Solid Dosage (OSD) pharmaceutical manufacturing plant. The ideal candidate should have in-depth knowledge of Quality Management Systems (QMS) and hands-on experience in managing production activities in compliance with cGMP and regulatory requirements.

Key Responsibilities:

Ensure compliance with QMS requirements in production operations.

Manage and maintain production documentation including BMR, SOPs, deviations, and change controls.

Monitor and review CAPA, deviations, OOS, and audit observations related to production.

Coordinate with QA, QC, and regulatory teams to ensure smooth operations.

Support qualification and validation activities for equipment and processes.

Implement best practices to ensure adherence to GMP, safety, and regulatory guidelines.

Train production staff on QMS and compliance requirements.

Support internal and external audits and regulatory inspections.

Desired Candidate Profile:

B.Pharm / M.Pharm or equivalent qualification.

5+ years of experience in OSD pharma production with strong QMS exposure.

Strong understanding of cGMP, QMS, and regulatory compliance.

Good documentation, analytical, and problem-solving skills.

Ability to work independently and lead a team effectively.

https://www.linkedin.com/in/satnam-singh-37b9b518/

Job Title:

Job Responsibilities

• Supervise day-to-day production activities in

  OSD, Capsule, and Tablet manufacturing plant

  .
• Ensure adherence to

  cGMP, SOPs, and regulatory guidelines

  during production.
• Monitor production processes to meet daily, weekly, and monthly targets.
  
• Maintain accurate documentation and batch records as per pharma compliance.
  
• Coordinate with QA, QC, Engineering, and Warehouse teams for smooth operations.
  
• Implement continuous improvement practices to enhance productivity and reduce wastage.
  
• Ensure proper training and guidance to operators and shop floor staff.
  
• Maintain strict compliance with

  EHS (Environment, Health & Safety)

  standards.

Key Skills & Competencies

• Strong knowledge of

  pharma production processes

  (OSD, Tablets, Capsules).
• Familiarity with

  regulatory audits (USFDA, MHRA, WHO, etc.)

  .
• Excellent leadership, team handling, and communication skills.
  
• Ability to handle deviations, change control, and CAPA.
  
• Good problem-solving and decision-making abilities.
  

Desired Candidate Profile

• 36 years of relevant experience in a reputed

  Pharmaceutical OSD plant

  .
• Hands-on experience in

  tablet/capsule manufacturing

  processes.
• Strong understanding of

  GMP compliance and documentation practices

  .
• Candidates with exposure to

  multinational pharma setups

  will be preferred.

https://www.linkedin.com/in/satnam-singh-37b9b518/

Job Title: OSD Packaging Supervisor

Industry: Pharmaceutical

Qualification: B. Pharma

Location: Bari Brahmana (Jammu)

Experience Required: 2 to 5 Years

Salary: Up to 5 LPA (Negotiable)

9796871050

Job Description:

We are seeking a skilled and detail-oriented OSD Packaging Supervisor to join our pharmaceutical team. The candidate should have experience in Oral Solid Dosage (OSD) packaging operations, ensuring compliance with GMP standards and regulatory requirements.

Key Responsibilities:

Supervise daily packaging activities of OSD products as per production schedules.

Ensure compliance with cGMP, SOPs, and regulatory guidelines during all packaging operations.

Monitor line clearance, in-process checks, and reconciliation of packaging material.

Handle and train packaging staff to maintain efficiency and quality standards.

Maintain documentation including batch packaging records, deviation reports, and logbooks.

Coordinate with quality assurance and production teams for smooth operations.

Implement safety measures and maintain housekeeping standards in packaging areas.

Support regulatory audits and inspections with packaging-related documentation.

Desired Candidate Profile:

B. Pharma degree is mandatory.

2 to 5 years of experience in OSD packaging operations in a pharma manufacturing setup.

Knowledge of blister, strip, and bottle packaging lines.

Familiarity with cGMP, QMS, and documentation practices.

Strong leadership, communication, and team management skills.

https://www.linkedin.com/in/satnam-singh-37b9b518/

Job Title: Granulation Operator

Industry: Pharmaceutical

Location: Bari Brahmana (Jammu)

Qualification: ITI / Diploma

Experience Required: 3 to 6 Years

Salary: Up to 4 LPA

9796871050

Job Description:

We are looking for an experienced Granulation Operator to join our pharmaceutical manufacturing unit. The candidate will be responsible for operating and monitoring granulation equipment and processes while ensuring compliance with cGMP and safety standards.

Key Responsibilities:

Operate and monitor granulation machines (RMG, FBD, multi-mill, sifter, etc.).

Perform granulation activities as per SOPs, BMR, and regulatory requirements.

Ensure proper cleaning, calibration, and maintenance of equipment.

Monitor critical process parameters (temperature, pressure, RPM, etc.).

Maintain accurate documentation of production processes and equipment logs.

Support in process validation and qualification activities.

Adhere to safety protocols, GMP standards, and quality guidelines.

Coordinate with production, maintenance, and QA teams for smooth operations.

Desired Candidate Profile:

ITI / Diploma in relevant discipline.

3 to 6 years of experience as a Granulation Operator in the pharmaceutical industry.

Hands-on experience in handling RMG, FBD, sifter, multi-mill, and related granulation equipment.

Knowledge of cGMP, documentation, and safety compliance.

Team player with good communication and problem-solving skills.

https://www.linkedin.com/in/satnam-singh-37b9b518/