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

Thermo Fisher Scientific -
Athlone, County Westmeath

Apply Now

Job details

Full-time

Qualifications

Biochemistry
Management
Bachelor's degree
Chemistry
Leadership

Full job description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards

Job Description

Group Leader –Biopharma

At PPD, part of Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer.

We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research, our work spans laboratory, digital and decentralized clinical trial services.
Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.
Location/Division Specific Information

Our PPD® Laboratory Services team has a direct impact on improving patient health through the expertise of scientists, industry thought-leaders and therapeutic guides. As the world leader in serving science, our laboratory professionals bring their commitment to accuracy and quality to deliver groundbreaking innovations.

Discover Impactful Work:
The role of Group Leader is to provide support to our Biopharma department by providing management and direction to a group of laboratory staff and resources for project activities and needs, overseeing daily operations to monitor quality and project timeliness, and assist in preparation and implementation of company policies, quality systems and training programs.

A day in the Life

Management of a team of analysts
Allocation, scheduling and managing laboratory resources for group's project activities and updates LIMS for project status. Reviews timesheet reports for billing accuracy.
Preparation, review and approval of study protocols, project status reports, final study reports and other project-related technical documents.
Designing experimental study and participates in technical troubleshooting.
Reviewing data for technical quality and compliance to protocols, methods and SOPs. Review and approve laboratory investigations, deviations, QA facility and data audits. Assists in client and regulatory authority audits.
Responding to client questions and needs; leads client technical meetings.
Assisting in preparation of proposals, project definition and pricing.
Coordinating and prioritizing project activities with internal functional groups (physical testing, analytical development, etc.) and support functions (QA, sample management, etc.)
Assisting senior group leaders and/or managers in their responsibilities.
Preparation and implementing SOPs and company operational policies. Ensuring adherence and making recommendations for quality system improvements.

Education and Experience

Educated to a bachelor's degree level in a relevant area, ie chemistry, biochemistry. 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.
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5+ years) or equivalent and relevant combination of education, training, & experience.
1+ year of leadership responsibility

Knowledge, Skills, Abilities

Management experience in the pharmaceutical, biotech or analytical contract laboratory industries
Stability/QC/analytical R&D/project and program management.
Direct supervision of technical staff.
Full understanding of GMP requirements, client SOPs, ICH guidelines, EP and USP requirements, EMA and FDA guidance's.
Knowledge and experience of a wide range of techniques, HPLC, UPLC, Electrophoresis (CE, iCE, SDS-PAGE), ELISA, spectrophotometry.

Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
Apply today! http://jobs.thermofisher.com

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

Accessibility/Disability Access
Job Seekers with a Disability: Thermo Fisher Scientific offers accessibility service for job seekers requiring accommodations in the job application process. For example, this may include individuals requiring assistance because of hearing, vision, mobility, or cognitive impairments. If you are a job seeker with a disability, or assisting a person with a disability, and require accessibility assistance or an accommodation to apply for one of our jobs, please submit a request by telephone at 1-855-471-2255*. Please include your contact information and specific details about your required accommodation to support you during the job application process.

This telephone line is reserved solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes, such as not being able to get into the career website, following up on an application, or other non-disability related technical issues will not receive a response.

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Refine Your Search

science shift team lead jobs

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

Director Global Costing Center of Excellence

Global Labelling Manager, Content (Neuroscience)

PM2 Manufacturing Manager (Days)

Global Labelling Associate Director, Content (Established Products)

Global Labelling Associate Director, Content (Oncology)

Manufacturing Analyst and Documentation Coordinator - Core 1

QC Microbiology Scientist

Supervisor, Laboratory Quality Control

Medical Advisor, General & Speciality Medicine

Finance Operations Lead

Staff Systems Engineer

Global Labelling Director, Content

Senior Scientific Engagement & Program Manager

Medical Registrar - UPMC Whitfield Hospital, Waterford

Associate Director, Global Publications & Foundational Content

Architect - Automation N 4D

SRE- Availability Engineer

Global Head of Talent Acquisition

Contamination Control Supervisor

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