Posted to MedZilla on 1/2/2018

Sunrise Systems Inc

US-DC, Scientist 17-12994-MZ


Title: Scientist

Location: Fort Washington, PA 19034

Duration: 12 Months contract

ID 17-12994

Position Summary:

· Provides testing, technical and troubleshooting support in the QC laboratories.

These functions include:

· Collection, processing, method development and testing of chemical components, bulk products, raw materials, packaging components, finished products, marketed product stability, in-process materials, scale up, validation and cleaning validations to conform with specifications and standard operating procedures (SOPs).

· Thorough knowledge of SOPs, USP and other applicable pharmacopeia.

· Possess foresight to recognize task needs and performs the trained task without the request of management.

· Reviews and/or writes the following documents: APR, SOPs, QSRs, Instrument qualification, protocol/report writing, trending and review/analysis of data.

· Performs statistical analysis in support of APRs, Stability, and Product Release.

· Complies with cGMPs, safety training and regulations.

· Performs more advance technical projects under the supervision of management.

· Maintains an environment of respect and teamwork with all coworkers.


· Under limited supervision and in accordance with all applicable federal, state and local laws/regulations, the Companies’ policies, procedures and guidelines, this position:

· Ensure quality and compliance in all my actions by:

· Attend GMP training on the schedule designated for my role and as appropriate for my role

· Adhere to strict compliance with procedures applicable to my role.

· Exercise the highest level of integrity in the tasks that I perform

· In a timely and prompt manner, identify report and seek correction for deviations noted in my workplace.

· Embrace a behavior of employee involvement and commitment to doing the job right the first time


· Be a Power User in the applicable systems and roles assigned.

· Utilize tools within MS office and other systems to improve business effectiveness

· Exposure to & working knowledge of electronic batch records and/or other automated processes/systems (labs)

· Working knowledge of SAP or ERP system; including other relevant systems per role

· Edits documentation (i.e. Standard Operating Procedures, work instructions) as necessary.

· Understanding of product family, product size and put-up, and product characteristics (color, viscosity) associated active and excipient.

· Provide support during regulatory inspections /audits as directed. Support may be in the form of scribes, runner, and document gathering.

· Strong working GMP knowledge. Communicates and identifies GMP gaps.

· Can participate in all types of audits & Inspections.

· Leads areas in ensuring all operations (processes) are completed in a compliant and safe manner.

· Wears the appropriate PPE when working in manufacturing and other hazardous working environments and advocates standards of safety.


· Bachelor’s Degree in Microbiology, Chemistry, Biology, Natural Science, Medical Technology, or related science is required

· Minimum 2 years of GMP/GLP quality control lab experience in a pharmaceutical and/or OTC and/or regulated environment is required.

· Capable of performing routine laboratory activities. Light to moderate lifting

· Basic knowledge/exposure of a LIMS system is preferred


Megha Verma | Team Lead- Talent Acquisition

Sunrise Systems Inc.

Transforming Business. Enhancing Careers

105 Fieldcrest Ave Suite# 504, Edison, NJ 08837 USA

Desk: (732) 272 0329

Email: [click here] | URL:

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