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职位1:
2 e q/ c, y3 j; wChemist /QC2 q/ W9 S. \+ q& e- R
Location: Las Vegas& m1 ~$ |3 L$ u8 K' f
Job type:Full time/part time
* n4 _& k& V6 H4 QSalary: DOE" W8 _7 d+ x1 y# s
Job Description:
" {0 o& J5 V# q) ?5 Q2 o1 M- The Chemist is responsible for the performance, recording and reporting of chemical tests of" ~6 s A9 j6 p
finished product, in-process, raw material, stability and validation samples of the Chemistry+ ^" O) ~( ]6 s" \8 M
Department. _/ x+ S0 m% f1 w# l& z
- Operate GC, HPLC, UV/VIS, FTIR, AA, pH, wet chemical equipment, Viscometer, scales, d9 j7 d+ i G; j! O
and other laboratory instruments as required by the applied test methods., T3 L. @- o, y/ b; N
- Perform and document the calibration of instruments, when required.8 t2 K: U+ Q1 ]$ s5 ^
- Assist in the requisition and inventorying of laboratory supplies.
4 a( K/ Q! w: x, w" }- Help with other tasks contributing to the overall operation of the laboratory as designated by- j+ X' {# a% F; r( R/ N2 `
the 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. u& l$ X) h/ C- {
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3 L/ X: J1 [6 T B$ Z0 n职位2:, f4 D, C, K9 i; ^9 L: G
Regulatory Affairs Associate1 ]0 p3 G' I7 K9 J" @
Location: Las Vegas
& R K/ a2 C8 xJob type:Full time/part time( y- \$ a# o3 H7 _2 Q( ]
Salary:DOE, J( O3 Y4 |" x8 w) h9 x
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Job Description:! ?! }7 I1 w9 u
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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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EDUCATION and/or EXPERIENCE: % E8 @( g; M* ?1 o M3 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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