Large Job Vacancies in New Jersey, USA

Apnar Pharma is a privately owned, rapidly growing pharmaceutical company. We are engaged in the acquisition, licensing, development (ANDA), sales, Manufacturing, marketing & distribution of generic pharmaceuticals, drugs, and OTC (over the counter) non-prescription items for U.S. market.

In addition to our strategic partnerships, we have a highly experienced team of professionals who all work together to provide quality medicinal products. Our team specializes in analytical development & analysis, formulation development, regulatory affairs, quality control, quality assurance, manufacturing, accounting, marketing, distribution, and finance

Production Supervisor

To handle all operation activities of Production, Packing and Warehouse department.

Area maintenance as per cGMP requirements and ensure compliance.

Daily job allocation and manpower handling.

Production planning and Materials arrangement to run routine production activities.

Exposure of audit inspection of USFDA and/or other regulatory agencies.

Handling of change control, deviation, CAPA and other QMS documents.

Installation and qualification of new equipment in production area.

Training to the staff and operators of production, packing and warehouse department

Engineering Mechanic

A Maintenance Engineer in a pharmaceutical company is responsible for ensuring the smooth and efficient operation of plant equipment and facilities, adhering to strict safety and regulatory standards.

Their primary role involves calibration, planning, executing, documenting and coordinating preventive and corrective maintenance activities to minimize downtime and ensure product quality.

QC Chemist

Analysis of raw material, packing material, in-process samples, finished product and stability samples.

Method verification of finished products, raw materials.

Preparation of STP, TDS and SOPs related to QC department.

Sampling of raw materials and packaging materials.

Calibration and verification of analytical instruments and equipment used in QC department

Granulation Operator

• Operate granulation equipment such as fluid beds, rotary dryers, and cooling tunnels to produce high-quality granules.
  
• Monitor and control the moisture content of granules during processing to ensure optimal product quality.
  
• Perform sieve analysis on finished products to meet specifications and reject any non-conforming materials.
  
• Maintain accurate records of production runs, including batch numbers, product yields, and quality control results.
  
• Collaborate with other operators to troubleshoot issues related to equipment malfunction or product variability.

Packaging Operator

• Assemble blister packs according to product specifications.
  
• Label products accurately and efficiently.
  
• Ensure proper sealing of bottles using caps or other closures.
  
• Collaborate with team members to meet production targets.

• Operation and cleaning of bottle packing line equipment like counter, cotton insertor, canister insertor, unscrambler, capping machine, induction sealer, labeling machine and serialization.

• Candidates also having Blister packing machine experience will be preferred.

• Ensure the cGMP, GDP, and data integrity compliance

Coating Operator

Operation and cleaning of autocoater machine.

Cleaning, dismantling and complete changeover of coating machine.

In-process checks during encapsulation activities.

Ensure the cGMP, GDP, and data integrity compliance

Tablet Press/ Encapsulation Operator

Operation of Compression machine with metal detector & Deduster machine.

Cleaning, dismantling and complete changeover of tablet compression machine.

Experience of bilayer compression machines will be an additional advantage.

In-process checks during compression activities.

Ensure the cGMP, GDP, and data integrity compliance.

Operation and cleaning of encapsulation machine with all line machines.

Cleaning, dismantling and complete changeover of encapsulation machine.

In-process checks during encapsulation activities

QA Supervisor

Preparation, review and approval of SOPs and GXP documents.

Issuance, review, approval and retrieval of BMR/BPR.

Follow GMP guidelines in the production area.

Exposure of audit inspection of USFDA and/or other regulatory agencies.

To handle training management system.

To handle the Process validation & cleaning validation activity.

To handle risk assessment, change control system, deviation, CAPA, OOS & OOT.

Line clearance, IPQA, Sampling activity

We are inviting candidates with a valid US Visa to apply for job opportunities for our manufacturing facility in the United States.

Applicants who do not hold a U.S. visa but are keen to work at a U.S. manufacturing unit may also apply

 

Email: hr@apnarpharma.in, customerservice@apnarpharma.com