188307 - QC Technician
Industry
MAN
Region
MA-Massachusetts
City
Bedford
State
MA
Rate
Up to $22.00 DOE
Duration
12 Months
Description
Chipton-Ross is seeking a QC Technician for an opening in Bedford, MA.

RESPONSIBILITIES:
The Intermediate QC Technician performs Quality Control functions independently or under moderate instruction including: analytical testing, inspection and release of raw materials; inspection of finished packaged goods; issuing of line clearances in support of manufacturing processes; data entry in SAP; water sampling and buffer preparation. The successful candidate will follow and adhere to in-house testing procedures and maintain compliance with ISO9001, ISO13485, safety and regulatory requirements as they apply to the laboratory and work areas. Minor local travel by car is required.

In addition, the Intermediate Technician functions as key member of the QC group and may support the following tasks:

Create deviations and OOS report, support root cause analysis and CAPA as requested.

Assist in writing and reviewing new and existing SOPs

Participate in and support Continuous Improvement Projects

Required to work on tasks of moderate scope where analysis of situations or data requires problem solving skills. Excellent written and oral communication skills are required. Must be self-motivating, detail oriented and comfortable working in a team-oriented environment and able to multitask in a fast-paced environment and prioritize work as necessary.

REQUIRED EXPERIENCE:
Must be able to work safely with chemicals, biologics and hazardous materials.
Compliance knowledge with ISO9001, ISO13485, ICH Q2, GMP/GLP requirements preferred.

Knowledge of Process Excellence, Six Sigma and Lean Manufacturing is a plus.

Must be able to work independently as well as work with a diverse team. Knowledge of SAP or similar inventory control systems desired. Familiar with Microsoft Excel and Word. Excellent oral and written communication skills are required to be effective in this role.

PREFERRED EXPERIENCE:
Experience with routine lab techniques such as RI, FTIR, UV/Vis analyses desired

Knowledge of Lean Manufacturing is a plus.

Experience with SAP is a plus

Experience with Trackwise is a plus

EDUCATION:
Accredited BS or higher in Chemistry, Biology, Biotech or related fields, with 1-3 years of experience in a Biotech/Pharma/Clinical QC environment.

WORK HOURS:
1st Shift
Full-Time

Employment will be contingent on clearing a drug screen and background check. Both must clear prior to start date.

Contact
Billy James
bjames@chiptonross.com
CHIPTON-ROSS, INC.
420 Culver Boulevard
Playa Del Rey, CA 90293

Phone: (310) 414-7800 x340 or (800) 927-9318 x340

Candidates responding to this posting must currently possess the eligibility to work in the United States. No third parties please.

Employment will be contingent on candidate clearing pre-employment drug screen and background check.

Chipton-Ross provides equal employment opportunities to all employees and applicants for employment without regard to race, color, creed, religion, national origin, sex (including pregnancy), age, disability, sexual orientation, gender identity and/or expression, protected veteran status, genetic information, or any other characteristic protected by Federal, State or local law. This policy governs all areas of employment at Chipton-Ross, including recruiting, hiring, training, assignment, promotions, compensation, benefits, discipline, and terminations.