Project Management Technical Expert

Project Management Technical Expert Bridgend, Wales

PCI Pharma Services
Full Time Bridgend, Wales 10.56 - 12.04 GBP Today
Job description

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.

We are PCI.

Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.

General Purpose of Role
:
To perform a Quality Operational role which supports:
  • Management and execution of all Quality Investigations and procedural updates that are the responsibility of the Project Management department within the European region
  • Maintain, support and improve the Pharmaceutical Quality System employed within PCI, specifically to improve procedures and implement CAPA’s in relations to PM procedures and processes, with zero overdue without an extension.
  • Maintain, support and improve completion of NMRs raised to ensure on time delivery of tasks and service
  • Collate and manage KPI’s and metrics and provide for Business Review Meetings.
  • A lead user for site QMS system within Project Management.
Main Responsibilities:
  • Support Project Management with investigating and drafting Quality Event Investigations within standard timelines
  • Ensure timely completion of deviation investigations in conjunction with Operations, PM, QC and QA departments.
  • Support in completing CAPA actions within standard timelines working with the appropriate departments to facilitate deviation closure.
  • Administration, control and support core systems within the Pharmaceutical Quality System as allocated by department manager. Including but not limited to: QIR/complaints, CAPA, Change control, NMR and document control systems.
  • Work closely with personnel to develop departmental technical writing skills and improve processes and procedures.
  • Reporting of metrics for systems within scope of responsibility, e.g Client BRM support.
  • Provide information and give feedback on progress of deviations/investigations that may impact batch release.
  • Attend deviation meetings and give appropriate feedback for deviation status and progression
  • Support delivery of site projects and objectives and be a representative for Project Management
  • Support the site’s Continuous Improvement activities and maturity index through the one PCI initiative.
  • Write Project Management related standard operating procedures, SOI’s and WI.
  • Ensure Training modules are kept up to date based on CAPAs implemented.
Specific Qualifications:
A HND or equivalent in a business, quality or life sciences subject and / or suitable experience within an operational, quality assurance or technical role within the pharmaceutical industry.
Previous Work Experience:
Essential
Meets one of the following requirements:
  • Experience in a Quality/Technical role within a regulated industry (pharmaceutical, biotechnology, medical device).
  • Experience in a Quality Assurance/Technical Writer role within a regulated industry with transferable skills (e.g. Aerospace, food, automotive)
  • Experience of technical writing, Root Cause Investigation and implementation of CAPA.
Desirable
  • Knowledge of cGXP, regulatory requirements and appropriate ISO standards.
  • Experience of Investigational Medicinal Products, Biotechnology and EU/US clinical trials is highly desirable.
Specific Knowledge / Skills Competence:
  • Strong written and verbal communication skills.
  • The ability to introduce, co-ordinate, complete and report on projects.
  • A high level of self-motivation is required
  • Able to rationally persuade and positively Influence
  • Ability to manage conflict and make sound scientifically based decisions.
  • IT literate (experience of e-QMS/document management systems and ERP systems desirable).
Join us and be part of building the bridge between life changing therapies and patients.
Let’s talk future
Equal Employment Opportunity (EEO) Statement:
PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

Project Management Technical Expert
PCI Pharma Services

www.pciservices.com
Philadelphia, United States
Salim Haffar
$25 to $50 million (USD)
1001 to 5000 Employees
Company - Private
Health Care Products Manufacturing
Related Jobs

All Related Listed jobs

Sales Development Representative - Entry Level
WatchMyCompetitor.Com London, England 22000 - 27000 GBP ANNUAL Today

Contacting prospective clients through outbound marketing to introduce our product - including phone, email and social media.

Band 6 High Intensity Trainee - Birmingham Healthy Minds
Birmingham and Solihull Mental Health NHS Foundation Trust Birmingham, England 35392 - 42618 GBP ANNUAL Today

Keele University will be the academic place of study for this Post Graduate Diploma in CBT and the expected mode of delivery will be face to face learning.

Commissioning Project Manager x 3
Slough Borough Council Slough, Berkshire, South East England, England 42503 - 47573 GBP ANNUAL Today

Salary: 42,503 to 47,573 per annum (pro rata) plus a Local Weighting Allowance of 1002 is also payable. Hours of work: Full time 37 Hours per week.

Nurses of Newcastle
Reactive Healthcare Newcastle upon Tyne, England 35000 - 38000 GBP ANNUAL Today

After your extensive training, you will telephone call claimants to build rapport & assess their needs & requirements, then generate a report based on your

Maintenance Supervisors
The Wrekin Housing Group Telford, England 37217 - 39398 GBP ANNUAL Today

The main purpose of this position is to supervise a team of operatives and heating engineers to deliver an excellent servicing and repairs service to our