vegas制药厂诚聘多位人才
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发表于 2017-12-20 10:54 | 只看该作者

vegas制药厂诚聘多位人才

制药厂, 生物科技, 招聘, 工厂, 薪资优

职位1：4 y" b" Z8 c! M  K% r
Chemist /QC
Location: Las Vegas
Job type:Full time/part time  c: h1 M" h0 g( R& x. B% L
Salary: DOE
Job Description:
- The Chemist is responsible for the performance, recording and reporting of chemical tests of
finished product, in-process, raw material, stability and validation samples of the Chemistry& N6 E. u; t+ w! N* I$ H/ Q7 p
Department.$ r- l. B, A2 b2 {. l: p1 w
- Operate GC, HPLC, UV/VIS, FTIR, AA, pH, wet chemical equipment, Viscometer, scales
and other laboratory instruments as required by the applied test methods.- [4 J% W& z3 F
- Perform and document the calibration of instruments, when required.
- Assist in the requisition and inventorying of laboratory supplies.; {. \* X  c, p0 m( c; `
- Help with other tasks contributing to the overall operation of the laboratory as designated by: e+ S* u6 m# M$ {5 T
the Chemistry Department Manager and Supervisor.( f8 u  L* t' I1 @5 s% e' p! u

EDUCATION and/or EXPERIENCE: Bachelor's degree (B.S.) Chemistry or related science degree from a college or university is required. Master/PhD degree is  preferred.One year industrial work experience in the chemistry laboratory is preferred.

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职位2：; U4 x; C2 O2 W) g9 Q
Regulatory Affairs Associate4 t/ Q! W, j6 X6 [; w) P! g
Location: Las Vegas0 n3 i- O( m& `% x; k0 m. f  m
Job type：Full time/part time
Salary：DOE) ^, |7 Q% Y2 o7 y* V
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Job Description:

Managing the activities as assigned for regulatory affairs and compliance throughout the business.
Ensuring a products quality during the production process and applicable regulations and procedures are adhered to (cGMP, ISO, FDA, FTC, etc.)
Serves as the company's most responsible contact for any necessary interactions with regulatory authorities.
Interact with domestic and foreign regulatory authorities in the same capacity as necessary. Interact with regulatory agencies to answer questions, plan meetings, obtain information, and otherwise facilitate regulatory interactions.
Create and maintain SOP’s, assist in training, lead all audits, assist in the research and development of new products and the continuous improvement of current products.
Be proactive to minimize or eliminate regulatory issues to help prevent any impact of adverse regulatory activities on the corporate reputation, market or bottom line.
Lead all audits required from regulatory agencies, customers and prospects.
Co-ordination with various stake holders, project teams, strategic sourcing, QA/QC, systems, supply chain, sales, equipment, facilities, project management to plan scale up activities in effective & timely manner.
Investigates, reviews, and recommends new procedures, policies and/or technology that would improve or enhance the department’s capability to deliver service, quality, compliance and build sales.

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EDUCATION and/or EXPERIENCE: ( n @, a: {: g' S; o3 B7 v8 I1 V4 q
Bachelor's degree (B.S.) Chemistry or related science degree from a college or university is required. Master/PhD degree is preferred. One year industrial work experience in the chemistry laboratory is preferred.

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