Pharmaceutical Production Release Pharmacists

 

Recruiter:

The Recruitment Agency South Africa

Job Ref:

TRASA Release Pharma..

Date posted:

Monday, February 8, 2021

Location:

PortElizabeth, South Africa

Salary:

Annual Salary


SUMMARY:
a Big Giant in the Pharmaceutical Industry is looking to employ skillful Release Pharmacists to join their dynamic team of experts urgently!!!

POSITION INFO:

Overview

Position: We are looking for 8x Pharmaceutical Production Release Pharmacists to join a Big Giant within the Pharmaceutical Industry urgently.

Salary: Market Related

Location: Port Elizabeth

Quality Assurance Department

Applicants are invitedto apply for this excellent opportunity that exists for the above mentioned position. The successful incumbent will report to the QA Manager.

Overview

Ensure in-process materials and finished products comply with GMP guidelines, regulation, and in-house SOPs. Determine product release for use into the marketplace, Control of documentation in compliance with regulation and company policies and procedures, and all administrative tasks.

Responsibilities

Planning and project support

§ Implement and coordinate systems and procedures and make decisions within policies and procedures, or as authorized by superiors

Product Release

§ Review batch documentation and production conditions to assess compliance to quality procedures, standards and product specifications

§ Review and approve quality of new, in-process and released batches to assess compliance to quality control programs, product specifications, and GMP guidelines

§ Approve and release production batches

§ Execute batch release priorities in line with OTIF and planning schedule

§ Ensure release requirements are met for finished products

§ Determine disposition of in-process and finished products for clinical and commercial use

§ Ensure changes/ deviations in production or quality control have been approved according to QMS

§ Initiate tests/ checks/ inspections/ sampling to mitigate any risk associated with planned changes/ deviations

§ Ensure production and QC documentation are completed in compliance with SOPs

§ Monitor and audit compliance to regulatory and in-house standards with regards to current GMP

§ Report observed deficiencies in process and follow up on corrective action

§ Investigate systematic quality problems and develop preventative plans, in conjunction with Production

§ Provide input into GMP-related

Reporting

§ Complete and consolidate standard documents

§ File, archive and retrieve documents

§ Maintain and update records and systems as required

Skills Required

§ 2 – 4 years’ experience in pharmaceutical product release and planning processes

§ Bachelor’s degree in Pharmacy

Specific job skills

§ Comprehensive knowledge of pharmaceutical manufacturing and corrective action programs

§ Pharmaceutical standards and compliance requirements

§ Ability to interpret and implement policies, processes and objectives

Competencies

§ Information Gathering

§ Interrogating Information

§ Meeting Deadlines

§ Finalizing Output

§ Taking Action

Benefits:

· Will be discussed

Application Deadline: 2021/02/05

Expected Start Date: 2021/04/01



 

NB! This job is now closed. You can apply for other jobs by uploading your CV.



 

 

 

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