Work Schedule

First Shift (Days)

Environmental Conditions

Office

Job Description

Location:

• Sweden
• Gothenburg (on site)

To start as soon as possible

**candidates must hold the right to work in Sweden **

At 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 through our PPD clinical research portfolio, 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.

Thermo Fisher's clinical research business is a leading global contract research organization and world leader in serving science. We are passionate, deliberate, and driven by our mission – to enable our customers to make the world healthier, safer, and cleaner.

Key responsibilities:

• Audits laboratory data for compliance with methods and standard operating procedures and report findings

• Audits sample result tables and analytical reports for completeness and accurate representation of the data and report findings

• Serves as a resource to operational departments on audit or quality assurance subject matter

• Assists in the preparation of audit findings and/or other related information

Education and Experience:

• Bachelor's degree or equivalent and relevant formal academic / vocational qualification; Associates' degree and relevant experience is acceptable in lieu of Bachelor's degree Previous QA or lab experience that provides the knowledge, skills, and abilities to perform the job (comparable to 1-2 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.

Knowledge, Skills and Abilities:

• Familiar with applicable GxP and appropriate regional regulations

• Thorough working knowledge of SOPs and WPDs

• Excellent oral and written communication skills (including appropriate use of medical and scientific terminology)

• Strong attention to detail

• Able to work independently or in a team environment

• Strong problem solving abilities

• Strong organizational and time management skills

• Basic computer skills and ability to learn and become proficient with appropriate software

• Proven flexibility and adaptability

• Valid driver's license and ability to qualify for and maintain a corporate credit card with sufficient credit line for business travel

Working Environment:

Below is listed the working environment/requirements for this role:

• Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.

• Able to work upright and stationary and/or standing for typical working hours.

• Able to lift and move objects up to 25 pounds

• Able to work in non-traditional work environments.

• Able to use and learn standard office equipment and technology with proficiency.

• May have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environments.

• Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.