Qc Inspector

focuses on inspecting product and conforming to release procedures ensuring

**that**:
All goods released are fit for purpose and
adhere to the customer specification
Customer quality expectations are met in full
by completing sample checks, relevant sign off checks as well as communicating,
recording, and investigating as appropriate quality related non-conformances.
Ensuring commitment to following Standard Operating Procedures in accordance
with ISO 9001 & PS9000 and the company’s best practice quality and safety
procedures.

**KEY ACCOUNTABILITIES**:
To
complete all final inspection duties and associated administrative tasks
to release goods on VWT as per customer specifications.
To understand, operate and adhere to the documented quality system operating procedures
To provide in process testing in accordance with SOP’s and customer specifications
To manufacture and control colour standards
To monitor and action calibration requirements
To carry out patrols and spot checks as required to support the identification of non-conforming products.

To
ensure existing technology is being optimised and used effectively to
support the manufacture of good quality product i.e., Barcode scans,
electronic work tickets signed and dated correctly.
To
ensure discrepancies are recorded and brought immediately to the attention
of Team leader/Quality Manager.

To support and advise all production departments of acceptable quality standards, making quality judgments considering individual customer quality requirements and follow due processes to prevent release of non-conforming product
To
review quarantined product and co-ordinate the 100% inspection of product
as and when required
Ensure appropriate
records are maintained and reports compiled
To
promote good manufacturing practice and champion good housekeeping
standards through routine inspections
To
train in new systems of work following changes to systems of working
caused by production or customer specification changes and ensure
adherence within production processes.
Support
the review of current processes and support in updating standard operating
procedures and support ongoing accreditation standards.

To
assist with non-conformance investigations and quality complaints in the
drafting and implementation of corrective and preventive actions (CAPA) as
required

To
assist in other areas of the business as required

Participate
in continuous development and training.

**KNOWLEDGE, SKILLS, EXPERIENCE AND QUALIFICATIONS**:
The ability to gain knowledge of the Pharmaceutical/Healthcare market requirements.

Able to become familiar with ISO 9001 & PS9000 quality standards and procedures.
Able to develop an understanding of acceptable quality levels for each customer.
A knowledge of GMP and potential problems and issues.
Sound process knowledge in a production environment and experience in a quality function is preferable.

The ability to work with mínimal supervision.

Basic computer skills.

Willing to learn new skills.

Methodical approach to undertaking tasks.

Problem solving skills.

**BEHAVIOURS**:
Ability to communicate effectively with internal and external customers.

Ability to overcome obstacles.

Be able to be self-motivated, standards driven, with a keen eye for detail.

Ability to use own initiative and lead by example.

Ability to remain calm under pressure and work to tight deadlines.

The ability to sort and input information with accuracy and speed.

Problem solving skills.

Initiative.

Thoroughness and a concern for standards.

Efficiency focused and attention to detail.

Results focused.
Uphold and promote WestRock’s Values and Behaviours.

Must be flexible and adaptable to change.

Must be prepared to take on additional responsibilities and other duties as required to meet business needs.

Successfully adapt to changing demands and conditions.