ACG Pharmapack Hiring Graduate in Pharmacy for Officer- Quality Regulatory-Apply Now

 ACG Pharmapack Pvt. Ltd Hiring 2022 Graduate in Pharmacy/Plastics / Chemistry  for Officer- Quality Regulatory At Shirwal, India . ACG Pharmapack Pvt. Ltd Notification full details below..Interested and eligible candidates can Apply Now.

  • Vacancy details:

  • Post Name: Officer- Quality Regulatory
  • Qualification: Graduate in Pharmacy/Plastics / Chemistry  
  • Experienced:6 to 8 years
  • Openings:NA
  • Salary:NA

Job Description: ACG Pharmapack Pvt. Ltd Hiring For Officer- Quality Regulatory ! 

  • Important Details :

  • Location: Shirwal, India
  • Post of date:01/07/2022
  • Selection ProcessThe selection will be on the basis of Interview.

Roles and Responsibilities

Primary Responsibilities

Strategic and planning
•    Establish compliance of certifications, product registration with regulatory bodies, performing regulatory testing to provide timely feedback to global customers.
•    Achieve Operational efficiency by monitoring qualification and validation of equipment’s and instruments through controlled change management process to facilitate high quality products.
•    Benchmark global target for ACG in terms of GMP in pharmaceutical primary packaging industry through periodic GMP audits of facility and conduct periodic GMP awareness trainings to all associates.
Core Functional
•    Ensure regulatory status of films and foils products by conducting applicable testing methods through external service providers. 

•    Liaise with consultants for DMF filings of products with regulatory authorities, annual updates and amendments of existing DMF, as and when required.

•    Regularly monitor & update the documentation required as per ISO, Food Safety & GMP requirements and timely updating and/or amending the same followed by periodic review of SOPs, WI and other QMS documents to ensure system compliance.
•    Prepare & maintain various documents (e.g., compliance certificates, LOAs, etc) required by customers with respect to the regulatory requirements & queries 
•    Ensure periodic Customer / certification Audit, ensure customer satisfaction & continuation of certifications by interacting and timely compliance to audit observations within stipulated timeframe.
•    Ensure effective implementation of vendor quality management by scheduling supplier audits, review audit reports, compliance of Regulatory documentation & periodic updates for adequacy in coordination with Purchase Team.
•    To ensure effective implementation of food safety management system as per responsibilities and authorities described in standard.
Internal Processes
•    Perform Self-inspections as per annual schedule, 
•    Ensure and monitor timely compliance and effectiveness of actions taken against internal/external audit findings.
•    Prepare technical agreement for all raw material suppliers and service providers.
•    Monitor qualification and validation activities of instruments, equipment’s and processes in line with validation master plan and validation procedure. 
•    Conduct periodic cGMP audits.
•    Maintain control of documents in terms of generation, amendment, issuance and cancellation as per defined SoP

Key Result Areas

•    Compliance of customer / certification audits in agreed timelines for continuation of business and certification.
•    Issuance of regulatory documentation and response to customer quires within timelines excluding new regulations.
•    Monitor & track change management system with timely documentation and effective implementation & closure within timeframe.
•    Ensure that the shop floor GMP practices are followed as per SOP to meet customer expectations on CGMP. Number of repeat instances of failure of GMP observations to be mapped to achieve the GMP score as per the internal score card norms.
•    Review and upgradation of ISO (QMS, EMS, FSMS & cGMP) & Regulatory documentation by involving cross functional departments within timeframe as applicable.
•    Carry out testing of films & foils as per the applicable test methods as part of regulatory testing through external laboratory, payment processing and preparation of complete and correct documentation as required for CFDA CDE / USFDA/ Health Canada registration. Annual updating of DMF registration.
•    Prepare IQ, OQ, PQ protocol & report format, monitoring of Qualification, validation activities, equivalency studies for new as well as existing equipment’s and instruments, change in composition of product formulation on shop floor in co-ordination with user department

Key Interfaces

Internal Interfaces:

  • Planning
  • Production
  • Safety
  • Human Resources
  • Purchase
  • Development & Technology
  • Sales
  • Business Development
  • Operational Excellence
  • Engineering.

External Interfaces:

  • Certification Agencies.
  • Regulatory Agencies.
  • Customers.
  • Suppliers and service providers.

Educational and Experience Requirements

Graduate in Pharmacy/Plastics / Chemistry with 6 to 8 years of relevant experience.


  • Postgraduate in Regulatory affairs
  • Certified ISO Lead auditor

Technical Competencies & Personas

worked on change control or Validation/Compliance roles in an organization to ensure CSV compliance / process compliance

Regulatory & Risk Management

Customer and Supplier Management

Handling ISO Audit, Supplier’s Re-Evalution and Aesthetic Audit




Has the candidate displayed any of the Values (Caring/Collaborative/Progressive) during the discussions?

How to Apply :

Step 1: Click on below link and you will be redirected to  Career Page of Recruiting Company or Career portal.

Step 2. Register on Career Page of the Company or  Career Portal by giving log in credentials and other personal or education details .

Step 3.Upon successful registration .User need to log in with credentials.

Step 4.Once logged in, User need to fill the all relevant personal ,educational  , Work experience details ,attach resume and submit application form.

Click here for notification and Apply

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