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标题: vegas制药厂诚聘多位人才 [打印本页]

作者: MERION    时间: 2017-12-20 10:54     标题: vegas制药厂诚聘多位人才

职位1:: v3 t2 h& Y/ P. h7 Y
Chemist /QC
! z& p' |( J3 B9 hLocation: Las Vegas0 \7 H4 d$ J/ I- z* \; e
Job type:Full time/part time+ e8 ^* d5 r7 F
Salary: DOE
$ ~5 i  ~+ l5 i2 s0 W+ JJob Description:' B1 o4 f' ~: y0 _# d3 |
- The Chemist is responsible for the performance, recording and reporting of chemical tests of% F0 T6 H) I8 L3 T
finished product, in-process, raw material, stability and validation samples of the Chemistry
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6 ?4 P; S2 {/ |3 S- Operate GC, HPLC, UV/VIS, FTIR, AA, pH, wet chemical equipment, Viscometer, scales* x/ N' p/ w# }) S& J" H
and other laboratory instruments as required by the applied test methods.
- M  ], @- U/ e8 q1 B/ h1 l- Perform and document the calibration of instruments, when required.  d" t. m, d( a
- Assist in the requisition and inventorying of laboratory supplies.8 J# C5 R- H- u5 B
- Help with other tasks contributing to the overall operation of the laboratory as designated by
4 G3 O& I: s  J5 uthe Chemistry Department Manager and Supervisor.
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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., }* t- n2 D8 E' V0 h1 y% e& }. X
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% j, R' w" U' p$ X" G5 u+ qRegulatory Affairs Associate+ `) ~% O! I1 c7 S9 I6 B
Location: Las Vegas
( Z. P$ ~- H. PJob type:Full time/part time) d, T6 c7 P- G$ `8 {
Salary:DOE7 c) \! G& I" w8 M3 X1 Y, y6 E
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Job Description:
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  • 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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. D% h+ X1 O( ^" Y7 `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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