Consumer Product Testing Company, Inc.
Sample Management Specialist/Client Services
Consumer Product Testing Company, Inc., Fairfield, New Jersey, us, 07004
Sample Management Specialist/Client Services
1 week ago Be among the first 25 applicants
Job Type:
Full-time.
Base Hours:
8:30 AM – 5:30 PM Monday through Friday
Minimum Qualification Requirements
To perform this job, an individual must be able to perform each essential duty satisfactorily, and meet the educational and experience requirements.
Essential Duties and Responsibilities
Responsible for receiving and documenting sample log-in. This includes all of the following:
Document the receipt of samples for analysis into the laboratory
Prepare study folders
Perform accurate labeling of samples
Update and maintain study folder revisions
Serve as client contact with regard to completion of authorizing documentation
Ability to work independently and as part of a team
Perform other tasks necessary to support site compliance to corporate and regulatory requirements. The Specialist ensures all related documents are fully and accurately completed in accordance with SOP’s, and applicable regulations including GMP, GLP, DEA, EPA, ISO 17025 and other relevant guidelines and standards.
Education and/or Experience
Associates’ degree in a related science OR equivalent with 1-3 years related experience is required.
Pharmaceutical Experience Is Preferred.
Strong organizational and problem solving skills to understand and carry out assigned duties effectively
Strong written and verbal communication skills and professionalism are required
Ability to work and adapt in a fast pace environment
Knowledge of regulations for drug/pharmaceutical environment is preferred
Must be detail-oriented and have the ability to multi-task
Microsoft Outlook, Excel and Word experience.
Sample handling experience (log, enter in database, create labels, etc.) is preferred.
Communication Skills
Must have strong communication and interpersonal skills.
Other Knowledge, Skills, and Abilities
Must have initiative and problem solving / analytical skills and keen attention to detail
Must have proficient computer skills in the following: Windows Word, and Excel
Must be organized, flexible, and able to work independently.
Applicant should possess the ability to organize and maintain all information for assigned projects and ensure adherence to established policies and procedures.
Physical Requirements of the Position
On an average 8-hour day this position requires the ability to walk, sit and stand, use hands to handle or feel, reach with hands and arms at or above shoulder height and below waist height, climb or balance, stoop, kneel, crouch; talk, hear, and smell. This position requires the ability to lift up to 40 pounds. Specific vision requirements including reading of written documents, visual inspection of materials and use of computer monitor screen frequently.
All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age or any other characteristic protected by law.
Seniority Level
Entry level
Employment Type
Full-time
Job Function
Other
Pharmaceutical Manufacturing
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Dover, DE $47,393.00-$62,386.00 5 days ago
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Administrative Assistant / Data Entry Clerk Franklinville, NJ $16.00-$20.00 6 months ago
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Job Type:
Full-time.
Base Hours:
8:30 AM – 5:30 PM Monday through Friday
Minimum Qualification Requirements
To perform this job, an individual must be able to perform each essential duty satisfactorily, and meet the educational and experience requirements.
Essential Duties and Responsibilities
Responsible for receiving and documenting sample log-in. This includes all of the following:
Document the receipt of samples for analysis into the laboratory
Prepare study folders
Perform accurate labeling of samples
Update and maintain study folder revisions
Serve as client contact with regard to completion of authorizing documentation
Ability to work independently and as part of a team
Perform other tasks necessary to support site compliance to corporate and regulatory requirements. The Specialist ensures all related documents are fully and accurately completed in accordance with SOP’s, and applicable regulations including GMP, GLP, DEA, EPA, ISO 17025 and other relevant guidelines and standards.
Education and/or Experience
Associates’ degree in a related science OR equivalent with 1-3 years related experience is required.
Pharmaceutical Experience Is Preferred.
Strong organizational and problem solving skills to understand and carry out assigned duties effectively
Strong written and verbal communication skills and professionalism are required
Ability to work and adapt in a fast pace environment
Knowledge of regulations for drug/pharmaceutical environment is preferred
Must be detail-oriented and have the ability to multi-task
Microsoft Outlook, Excel and Word experience.
Sample handling experience (log, enter in database, create labels, etc.) is preferred.
Communication Skills
Must have strong communication and interpersonal skills.
Other Knowledge, Skills, and Abilities
Must have initiative and problem solving / analytical skills and keen attention to detail
Must have proficient computer skills in the following: Windows Word, and Excel
Must be organized, flexible, and able to work independently.
Applicant should possess the ability to organize and maintain all information for assigned projects and ensure adherence to established policies and procedures.
Physical Requirements of the Position
On an average 8-hour day this position requires the ability to walk, sit and stand, use hands to handle or feel, reach with hands and arms at or above shoulder height and below waist height, climb or balance, stoop, kneel, crouch; talk, hear, and smell. This position requires the ability to lift up to 40 pounds. Specific vision requirements including reading of written documents, visual inspection of materials and use of computer monitor screen frequently.
All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age or any other characteristic protected by law.
Seniority Level
Entry level
Employment Type
Full-time
Job Function
Other
Pharmaceutical Manufacturing
Referrals increase your chances of interviewing at Consumer Product Testing Company, Inc. by 2x
Get notified about new Client Services Representative jobs in
Fairfield, NJ .
Dover, DE $47,393.00-$62,386.00 5 days ago
Vineland, NJ $37,000.00-$44,000.00 1 week ago
Administrative Assistant / Data Entry Clerk Franklinville, NJ $16.00-$20.00 6 months ago
We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr