Quality Control Inspector - Southern Suburbs Verfied

Salary Negotiable Southern Suburbs, Western Cape Southern Suburbs, Western Cape more than 14 days ago 05-10-2021 7:03:16 AM
15-10-2021 7:44:29 AM
A distributor of pharmaceutical products in Muizenberg would like to appoint a Quality Control Inspector who would be responsible for ensuring incoming goods, in-process and final product inspections are conducted, recorded and reported.

Duties and Responsibilities include, but are not limited to, the following:
DUTIES AND RESPONSIBILITIES:


Incoming Inspections (critical and non-critical components)

Critical Components

? Incoming inspections of foiled pouches received. Inspection and confirmation of batch Number, manufacturing date, expiry dates and revision control.
? Product packs to be sampled, compared and proofread according to the BOM’s and/or approved revision artwork.
? IFU’s to be sampled, compared and proofread according to the BOM’s and/or approved revision artwork.
? Care cards to be sampled, compared and proofread according to the BOM’s and/or approved revision artwork.
? Verification of Buffer solution received from supplier.
Non-critical components

? Visual inspections to be conducted on disposable bags for exterior quality conformity.
? Visual inspections on labels, boxes and any other non-critical components.
In-process inspections

? Perform visual and dimensional inspections on products, sub-assemblies and raw materials.
? Responsible for line openings and/or verifications.
? In process inspections to be done at intervals as per the company’s SOP.
? In process weighing to be done regularly in assembly rooms. Quarantined product boxes must be checked, recorded and rectified.
? Torque tests to be conducted and recorded at specified intervals.
? Leak tests to be conducted with use of vacuum chamber at specified intervals.
? Weighing of buffer bottles to ensure filling specification is met.

Documentation and training

? Ensure compliance of batch records supporting documents with internal procedures and GDP (Good documentation Practices).
? Assist with documentation and procedural changes as needed.
? Assist QA with training requirements for staff.
General

? Interface with production team to ensure expedited closure of issues/discrepancies detected during batch records review.
? Provide input for continuous improvement of procedures, specifications and processes.
? Ensure QC workstations are kept neat and tidy.
? Follow any lawful and/or reasonable instruction given by management.

EXPERIENCE AND KNOWLEDGE:

• Grade 12 or equivalent with math’s and science as subjects.
• At least 2 years working experience in a FMCG, Medical and or Pharmaceutical company.
• Knowledge of GMP and GDP would be advantageous.
• A certificate/Diploma QMS or equivalent would be advantageous.

SKILLS AND ABILITIES:

• Ability to work in a team environment
• Communication skills
• Work Standards (setting high goals or standards of performance for self and the organization.)
• Tolerance for Stress (stability of performance under pressure)
• Energy (maintaining a high activity level)
• Attention to Detail
• Integrity (Maintaining social, ethical and organizational norms in job-related activities)