Day-to-day responsibilities
* Management of quality critical PQS processes relating to documentation (e.g. SOPs, WIs, generation of manual Cs of A, archiving, specifications), ensuring compliance with regulatory requirements and the needs of the broader business.
* Issuing of company quality documentation (i.e. SOPs, WI, Logbooks).
* Applies the principles of continuous improvement by identifying and actioning improvements and efficiencies in the Processes for control and administration of documentation.
* Support of Quality Systems processes (i.e. CAPA, Change Control).
* Management of Departmental Reports.
* Generation of manual C's of A
Skills/Experience
* Educated to A Level standard (or equivalent).
* Minimum 1-2 years' experience working in a Quality Systems/Pharmaceutical environment.
* Good understanding of data integrity.
* Familiarity with Microsoft Office software.
* Knowledge of EU regulatory guidelines relating to the control of documentation.
* Good attention to detail with an analytical approach to work.
What we offer you
* A competitive salary
* Holiday – 25 days rising to 30 with length of service plus bank holidays
* Holiday Buy/Sell – an opportunity to buy or sell up to an additional 5 days holiday
* 3% Bonus - In addition to our competitive salaries, all our employees are entitled to join a discretionary bonus scheme (based on policy eligibility)
* Bravo Benefits Platform – offering a variety of discounts across well-being and lifestyle
* Salary Sacrifice scheme for Electric vehicles with Tusker (dependent on meeting policy eligibility)
* Medicash health cash plan
* Pension Scheme
* Life Assurance
* Employee recognition scheme
* The opportunity to develop your skills in a collaborative and supportive environment
At Ethypharm, we recognize the value of diversity in the workplace and provide equal opportunities for all. We are always open to discussing flexible working arrangements where this meets the needs of our business.
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