Company Information

You Matter to Cambrex.

Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance, drug product, and analytical services across the entire drug lifecycle. With more than 40 years of experience and a growing team of over 2,000 professionals servicing global clients, Cambrex is a trusted partner in branded and generic markets for API and dosage form development and manufacturing.

Your Work Matters.

At Cambrex, we strive to build a culture where all colleagues have the opportunity to:

• engage in work that matters to our customers and the patients they serve

• learn new skills and enjoy new experiences in an engaging and safe environment

• strengthen connections with coworkers and the community

  We’re committed to attracting and nurturing a passionate team of valued professionals in our fast-paced and growing company. We offer a competitive benefits package that includes healthcare, life insurance, planning for retirement, and more!

  Your Future Matters.

  Known for our customer-focused scientific and manufacturing excellence, as well as our strong commitment to quality and safety, we offer a range of career and growth opportunities across our global network of locations. Together with our customers, we aim to improve the quality of life for patients around the world. Start a career where You Matter by applying today!

Job Overview

As a Sample Management Technician in a combination role, you work with sample packages for the laboratories and support laboratory operations in the Analytical Services Department. This role may also interact with clients and regulatory agencies as part of audits.

This role will be a blended position with an approximate 75:25 mix of sample management responsibilities and laboratory support activities. Laboratory support includes glassware management, standard inventory and 6S, and may support routine laboratory tasks such as balance calibration and cleaning/maintaining of incubators and chambers.

Responsibilities

• Maintain custody of Received Sample Packages so that they are securely stored prior to the samples being logged in

• Unpack and inspect received Sample Packages

• Safely handle potentially hazardous and/or biologic material

• Review all Submitted Sample Paperwork (SSP) for accuracy and completeness.

• Download data from temperature monitoring devices and provide these data to the client/shipper, when appropriate

• Complete and return receipt acknowledgement of samples, when appropriate

• Store samples at indicated environmental temperatures

• Maintain and archive of the Submitted Sample Paperwork (SSP)

• Maintain cleanliness and organization of Sample Storage Areas

• Compile sample-specific documentation to accompany samples being shipped

• Communicate with analytical team members about samples and standard management

• Assist in reagent inventory and interact with vendors/place orders

• Wash glassware and manage glassware inventory

• As needed, maintain glassware washing equipment and collaborate with other departments to perform checks and qualifications

• Support sample shipment preparation and aliquoting of materials in GMP

• Support cleaning and maintenance in accordance with 6S principles.

• Cleaning of incubators and chambers requiring Biosafety Level 2 training

Qualifications/Skills

• Time and project management skills

• Excellent interpersonal skills, with ability to interact effectively and work efficiently with people at all levels in an organization

• Experience in writing and reviewing GDP documentation

• Experience writing SOPs and creating forms

• Familiar with LIMS systems

• Proficient in Microsoft Excel and Word

• Proficiency on technical operating systems

• Proven problem solving and troubleshooting abilities

• Effective oral and written communication skills

• Proven ability in technical writing skills

Education, Experience & Licensing Requirements

• Associates or Bachelor's degree or equivalent and relevant formal academic / vocational qualification

• Previous related laboratory experience that provides the knowledge, skills, and abilities to perform the job. Prefer 2+ years related experience in a GMP facility.

• Supervision Received:

  Works under general supervision.

  Physical Demands, Work Environment, and Travel

  Physical Demands

  The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

  While performing the duties of this Job, the employee is regularly required to use hands to finger, handle, or feel; reach with hands and arms; talk or hear and smell. The employee is frequently required to sit. The employee is occasionally required to stand; walk and stoop, The employee must be able to regularly lift and/or move up to 10 pounds, and occasionally lift and/or move up to 25 pounds. Specific vision abilities required.

  Environment and Protective Equipment

  The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

  While performing the duties of this Job, the employee is occasionally exposed to moving mechanical parts and vibration. The noise level in the work environment is usually very quiet.

  Travel:

  Little to no expected travel time.

  All requirements are subject to possible modifications to reasonably accommodate individuals with disabilities.

  Cambrex is an Equal Opportunity / Affirmative Action employer and will consider all qualified applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, age, protected veteran status, or disability status.