Manufacturing associate Work, Jobs in Send, Sry (with Salaries)

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Clinical Trial Supplies Associate Farnborough, UK

Syneos - Clinical and Corporate - Prod -
Farnborough

Apply Now

Job details

Full-time

Qualifications

Logistics
English
Microsoft Office Suite
Good Clinical Practice (GCP)
Good Clinical Practice (ICH-GCP) guidelines

Full job description

Clinical Trial Supplies Associate ** Farnborough, UK **

Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress.

Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape.

Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver – for one another, our customers, and, most importantly, for those in need.

Discover what your 25,000 future colleagues already know:

Why Syneos Health

We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
We are committed to building an inclusive culture – where you can authentically be yourself. Central to this is our purpose – Driven to Deliver – which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone’s life.
We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress.

Job Responsibilities

JOB SUMMARY

Performs administrative and support activities, as assigned by the Clinical Trial Supplies Manager (CTSM) or Project Lead (PL), to help manage the logistics of clinical trial supplies (e.g., batch review, customs clearance, supply and return).

JOB RESPONSIBILITIES

Assists in the development of systems and plans for distribution, re-supply, and return of clinical trial supplies.
Supports the review of batch manufacturing and packaging records to enable batch disposition.
Supports review and forecasting of inventory levels for all clinical trial supplies, in cooperation with project teams and project vendors

QUALIFICATION REQUIREMENTS

Associate’s Degree (or equivalent) level of education, preferably focused on life sciences

Experience in a contract research organization (CRO), pharmaceutical, or biotechnology company preferred

Knowledge of Good Clinical Practice, ICH guidelines, Good Manufacturing Practice, and other applicable regulatory requirements

High level of competence in English language

Proficiency with MS Office Applications

Ability to travel as necessary (up to 5%)

Disclaimer : Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.

Get to know Syneos Health

Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.

No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.

http://www.syneoshealth.com

Additional Information

Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.

Apply Now

Refine Your Search

manufacturing associate jobs in send, sry

Clinical Trial Supplies Associate Farnborough, UK

Quality Assurance & Regulatory Affairs Executive - Maternity Cover

Client Services Associate Project Manager Packaging

Clinical Trial Supplies Associate Farnborough, UK

Product Development Scientist

Project Manager - pharmacy robots (field-based) UK wide

Quality & Food Safety Specialist

Shift Critical Environment Technician

Store Associate - 'The Ordinary' - Seven Dials

Counter Associate - 'The Ordinary' - Selfridges, Oxford Street

Pharmaceutical Project Manager

Product Manager - Peripheral Vascular Disease

APM MONACO - Sales Associate - Part Time - London Selfridges

Control Systems / CSV Expert

Sales Specialist, Peripheral Vascular Disease - South West & South Wales

Containment Manager BPU (ID4817)

Health, Safety & Environment (HSE) Senior Specialist

Composite Supplier Quality Engineer

Field Service Engineer - East England

Personal Assistant / Office Manager

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