Find Quality ppd Jobs in Athlone County Westmeath

Compliance Specialist
Thermo Fisher Scientific —Athlone, County Westmeath
- Full-time
- Bachelor's degree
- No degree
- Computer skills
Supervisor (People Manager), Biopharma - Athlone, Ireland
Thermo Fisher Scientific —Athlone, County Westmeath
- 8 hour shift
- Presentation skills
- Bachelor's degree
- No degree
Supervisor, Pharma labs
Thermo Fisher Scientific —Athlone, County Westmeath
- Overtime
- Presentation skills
- Bachelor's degree
- No degree
Group Leader, Biopharma (Core day shift) - Athlone, Ireland
Thermo Fisher Scientific —Athlone, County Westmeath
- Full-time
- Management
- Bachelor's degree
- No degree
Scientist II, Biopharma - Core or evening shift
Thermo Fisher Scientific —Athlone, County Westmeath
- Full-time
- Bachelor's degree
- No degree
Assistant Metrologist
Thermo Fisher Scientific —Athlone, County Westmeath
- Full-time
- Clinic
- No degree
Scientist III (Pharma)
Thermo Fisher Scientific —Athlone, County Westmeath
- Full-time
- Analysis skills
- Bachelor's degree
- No degree
Senior Group Leader - Cell Lab
Thermo Fisher Scientific —Athlone, County Westmeath
- Full-time
- Management
- Presentation skills
- No degree
Scientist III (Inhalations)
Thermo Fisher Scientific —Athlone, County Westmeath
- Full-time
- Analysis skills
- Bachelor's degree
- No degree
Scientist III (LCMS Pharma)
Thermo Fisher Scientific —Athlone, County Westmeath
- Full-time
- Bachelor's degree
- No degree
7d
Business Manager
Thermo Fisher Scientific —Athlone, County Westmeath
- Full-time
- Bachelor's degree
- In-person
- Communication skills
4d

I want to receive the latest job alerts for quality ppd in athlone county westmeath

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

quality ppd jobs near athlone county westmeath

Senior Scientist jobs in Athlone, County Westmeath

Harris Group jobs in Dublin, County Dublin

Bright Motor Group jobs in Dublin, County Dublin

Group Leader jobs in County Dublin

Social Care Team Leader jobs in County Kildare

Internal Audit Manager jobs in Dublin, County Dublin

Revenue Manager jobs in Dublin, County Dublin

Housekeeping Manager jobs in Dublin, County Dublin

Project Manager Pharmaceutical jobs in Dublin, County Dublin

Senior Scientist jobs in Galway, County Galway

Senior Scientist jobs in Dublin, County Dublin

Senior Marketing Executive jobs in County Dublin

Kepak Group jobs in Fermoy, County Cork

Senior Scientist jobs in Naas, County Kildare

Senior Occupational Therapist jobs in Dublin, County Dublin

Senior Financial Accountant jobs in Dublin, County Dublin

Senior Physiotherapist jobs in Dublin, County Dublin

Senior Scientist jobs in Cork, County Cork

Senior Scientist jobs in Dundalk, County Louth

Medical Laboratory Scientist jobs in Dublin, County Dublin

Compliance Specialist

Thermo Fisher Scientific -
Athlone, County Westmeath

Apply Now

Job details

Full-time

Qualifications

Bachelor's degree
Computer skills
Communication skills
Time management

Full job description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as a Compliance Specialist - Make an Impact at the Forefront of Innovation!

Position overview:
The Compliance Specialist executes quality and compliance processes across the organization and facilitates the tracking and reporting of quality and compliance activities.

A Day in the Life of a Compliance Specialist:

Manages and leads all activities associated with project specific clients, regulatory, vendor, quality management, system, and/or internal audits and investigations to include: Develops updates and disseminates SOP’s/WPD’s as they relate to quality processes.
Performs internal and external audit related activities as needed and escalates significant issues appropriately.
Continually ensures audit readiness of client files.
Contributes to quality process improvement activities to ensure PPD meets or exceeds client expectations for the implementation of quality management systems and processes.
Ensures full compliance with CRG's procedures pertaining to quality investigations, quality audits and quality improvement initiatives.
Provides mentorship and guidance to less experienced quality staff.
Develops and maintains Client Product Specification Files
Completes a Quality Review of Drug Product Manufacturing Records and prepares Release Documentation for the Qualified Person.
Acts as the primary contact with customers on all aspects of GMP quality, the negotiation and management of customer Technical/Quality Agreements, the review of supporting documentation such as protocol, specifications, study summary etc. communicated directly with customer representatives to determine specific requirements and concerns, assume the lead in investigations and assure prompt responses to customer complaints and non-conformances, follows up to assure CAPA’s are implemented, tracked and closed in a timely manner plus assisting in hosting customer audits.
Conduct audits or activities in area of expertise
Provide project specific training to QA and/or manufacturing staff as applicable
Acts as lead on client projects
Maintain knowledge of regulations, SOP’s, QA departmental policies and procedures and demonstrate proficiency with audit procedures and proper documentation, in addition to knowledge in his/her area of expertise.
Conduct audits or activities in area of expertise, e.g. review quality system and batch production records.
Participates in client and regulatory inspections/audits and represent QA and following up on audit issues and corrective action.
Participates in inter-departmental meeting and contribute to policy-making decisions.

Education & Experience Requirements:

Bachelor's degree or equivalent and relevant formal academic / vocational qualification
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years).
In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Required Knowledge, Skills, Abilities:

Excellent oral and written communication skills
Solid organizational and time-management skills
Thorough knowledge and experience of the clinical trial process and GMP requirements
Thorough knowledge and understanding of ICH GCP and other relevant regulations and guidelines
Effective problem solving skills
Strong attention to detail
Ability to work independently as required
Strong computer skills; ability to learn and become proficient with appropriate software
Ability to multitask and prioritize competing demands/work load
Demonstrated flexibility and adaptability

Why Join Us?
When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference.

Apply today to help us deliver tomorrow’s breakthroughs!

Apply Now

Refine Your Search

quality ppd jobs in athlone county westmeath

Compliance Specialist

Supervisor (People Manager), Biopharma - Athlone, Ireland

Supervisor, Pharma labs

Group Leader, Biopharma (Core day shift) - Athlone, Ireland

Scientist II, Biopharma - Core or evening shift

Assistant Metrologist

Scientist III (Pharma)

Senior Group Leader - Cell Lab

Scientist III (Inhalations)

Scientist III (LCMS Pharma)

Business Manager

I want to receive the latest job alerts for quality ppd in athlone county westmeath

Explore jobs in more locations

Jobseeker tools

Employer Tools

Browse

Stay Connected