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American Society for Quality

Section 0102

Merrimack Valley

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The Merrimack Valley
section (# 0102) covers
NE Massachusetts and
SE New Hampshire

Established 1961

The section typically meets from Sept-June on the first Thursday of the month.

American Society for Quality
Merrimack Valley Sec. 0102
PO Box 275
North Andover, MA 01845-0275


This sight maintained by:

Jack Gale

 

 

 

 

 

 

 

 

 

 

 

 

 

 

CAREER PAGE

The Career Page is a free service of the Merrimack Valley Section. Positions available and positions wanted copy must be no larger than 1/2 column (5 inches high by 3.75 inches) and must be emailed. Space considerations require that Career Page copy will only be included if space is available and in the order received. Copy may be edited to meet space requirements. Listings typically will remain posted for two months.  Submit here

Latest New Postings: 28 June 2005

ASQ Career Page


 

Quality Engineer

PartyLite Gifts, Inc.

 

SUMMARY 

 

The primary purpose of this position is to provide technical input into the Product Development process.  Partnering with the PD team, the engineer will ensure PartyLite products are developed in a timely manner and include the necessary criteria that provide customer satisfaction.

ESSENTIAL DUTIES AND RESPONSIBILITIES
With Product Marketing and Research, Quality Assurance, and Global Sourcing lead the product specification development process in accordance to established timelines.

Provide technical input to the creation of the product / packaging specifications and standards.  Work with suppliers, cognizant of processes and control points, to assure manufacture of product to specifications and performance, including product stability.

 

Prepare written critiques on vendor submitted samples for product and package as compared with PartyLite standards.

 

Communicate product status (pass / fail) on samples and production submissions to all customers.

 

Accountable for product performance to meet specifications and requirements.

 

Other duties as assigned by Director of QA.

 

SUPERVISORY RESPONSIBILITIES

There are no supervisory responsibilities at the present time.

 

QUALIFICATIONS
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.  The requirements listed below are representative of the knowledge, skill, and/or ability required.  Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

 

EDUCATION and/or EXPERIENCE

Bachelor’s degree (BS/BA) from four – year college or university; and four to six years of business- related experience and /or training; or the equivalent combination of training and relevant business experience.

 

·        Consumer Products - Experience with glass, metals, ceramics, coatings, adhesives

·        Product / Process Engineering; New Product Development, Quality Engineering

·        Desirable experience: QS9000 (control plans, FMEA, QFD), 6 sigma, ISO 9000, TQM, SPC, DOE, APQP

·        Computer skills: MS Office

 

LANGUAGE SKILLS: Ability to read, analyze, and interpret general business periodicals, professional journals, technical procedures, or governmental regulations.  Ability to write reports, business correspondence, and procedure manuals.  Ability to effectively present information and respond to questions from groups of managers, clients, customers, and the general public.

 

 

MATHEMATICAL SKILLS:  Ability to apply advanced mathematical concepts such as exponents, logarithms, quadratic equations, and permutations.  Ability to apply mathematical operations to such tasks as frequency distribution, determination of test reliability and validity, analysis of variance, correlation techniques, sampling theory, and factor analysis.

 

 

REASONING ABILITY Ability to define problems, collect data, establish facts, and draw valid conclusions. Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables.

 

 

CERTIFICATES, LICENSES, REGISTRATIONS Desired: ASQ CQE or Reliability Engineer

 

PHYSICAL DEMANDS  The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

 

WORK ENVIRONMENT  The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

 

Ann Robertson

Staffing and Employment Manager

e-mail: ARobertson@partylite.com

www.partylite.com , a division of Blyth, Inc. www.blyth.com.

PartyLite Gifts, Inc.
59 Armstrong Road
Plymouth, Massachusetts
Tel: 508-830-3100
Fax: 508-732-5818

 

 

Posted 5/26/2005


 

 

 

 

 

 

 

 

 

Quality Manager

Via Wire Resources, Worcester area

 

A small, rapidly expanding manufacturer with 95 employees is actively seeking a QA Manager. The firm produces custom engineered products marketed to OEM’s in the medical, automotive and electronics industries. Reports to the COO, an individual with a reputation for excellent communication and leadership skills.

 

Their facility is modern, their financial condition strong. Position requires a hands-on individual with the technical and interpersonal skills necessary to advance QA to a highly effective, state-of-the-art function. Ability to work with shop floor personnel is essential. Experience in the medical or automotive industry a plus. The new QA Manager will feel comfortable in a change agent role, will be someone who wants to make a difference, a team-player with a positive and flexible disposition who will relish a challenge.

 

Contact:

 

Jack Cutler jcutler@wireresources.com
Wire Resources, Inc.
203.622.3000  ext 21
800.394.WIRE
www.wireresources.com

 

Posted 6/1/2005


 

QA Specialist-GCP Compliance
Idenix Pharmaceuticals

 

Idenix seeks individual with 3-5 years experience in quality assurance oversight of GCP compliance. Experience with QA oversight of Clinical Data management a plus.

 

  • Work with Idenix Clinical Staff to identify and draft Clinical SOP’s to assure GCP compliance.
  • Work with Idenix Data Management Dept to identify and draft critical SOP’s to assure GCP compliance
  • Perform Internal QA Audits of key systems & processes (e.g . SAE Reporting)
  • Perform Internal QA Audits of Clinical Studies (essential documents etc.)
  • Provide QA audits of Clinical Study Reports
  • Perform Internal Audits of Idenix Data Management Systems and Databases
  • Perform On-site GCP Audits of Investigators
  • Perform On-site GCP Audits of CRO’s
  • Aid or provide back-up to QA GMP compliance and Document Control as necessary.

Idenix offers an excellent benefits package including competitive salary, equity compensation, major medical insurance, dental insurance, 401(k) plan participation, and group life and disability insurance.

To be considered for this position, please send your resume by email to hr@idenix.com, or by mail to:

Human Resources
Idenix Pharmaceuticals
60 Hampshire Street
Cambridge, MA  02139

www.idenix.com

Posted 5/25/2005