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Christopher Sime Email & Phone Number

Senior Manager Quality Engineering at KINOVATE LIFE SCIENCES, INC
Location: Carlsbad, California, United States 12 work roles 3 schools
1 work email found @bachem.com LinkedIn matched
✓ Verified July 2026 4 data sources Profile completeness 100%

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Work email c****@bachem.com
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Current company
Role
Senior Manager Quality Engineering
Location
Carlsbad, California, United States
Company size

Who is Christopher Sime? Overview

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Quick answer

Christopher Sime is listed as Senior Manager Quality Engineering at KINOVATE LIFE SCIENCES, INC, a with 32 employees, based in Carlsbad, California, United States. AeroLeads shows a work email signal at bachem.com and a matched LinkedIn profile for Christopher Sime.

Christopher Sime previously worked as Senior Manager Quality Engineering at Nitto Denko Corporation and Quality Engineering Manager at Nitto Denko Corporation. Christopher Sime holds Bachelors, Biomedical/Medical Engineering from Hartwick College.

Company email context

Email format at KINOVATE LIFE SCIENCES, INC

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csime@bachem.com
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Profile bio

About Christopher Sime

10 years of Quality, Validation, process and Analytical Chemistry experience including FDA remediation and clinical trials. Research development of new product is a passion along with the desire for self improvement and education. Specialties: Knowledge of most laboratory equipment maintenance and use in a scientific environment. including validation testing and production. Developments multiple calibration and validation labs, document systems and equipment lifecycle programs.

Listed skills include Laboratory Equipment, Laboratory, Hplc, Organic Chemistry, and 41 others.

Current workplace

Christopher Sime's current company

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KINOVATE LIFE SCIENCES, INC
Kinovate Life Sciences, Inc
Senior Manager Quality Engineering
Carlsbad, CA, US
Website
Employees
32
AeroLeads page
12 roles

Christopher Sime work experience

A career timeline built from the work history available for this profile.

Senior Validation Engineer Iii (Supervisor)

Abbott Park, Illinois, Us

Contract position involving quality and validation remediation

Dec 2018 - Feb 2020

Senior Validation Engineer Ii

Abbott Park, Illinois, Us

Aug 2018 - Dec 2018

Qa Validation Ii

Bubendorf, Ch

May 2017 - Aug 2018

Validation Qa

Bubendorf, Ch

Under minimal supervision, responsible for a variety of production and non-production functions in support of manufacturing goals.Ensure product quality in all manufacturing operations by being alert and observant to detect problems and/or potential problems with equipment or productResponsible for running in-process, raw material release, calibration, and experimental devices, notifying appropriate personnel of results and completing all associated documentationResponsible for scheduling of testing activitiesResponsible for training and the documenting of training for all testing personnelResponsible for the completeness and accuracy of manufacturing documents and lab notebooksResponsible for retrieving and compiling data associated with all device testing and notifying the appropriate personnel if results are not in complianceResponsible for inventory accuracy of all testing related materialsInitiate and investigate Non-conforming Material Reports, Planned Deviations and Unplanned deviations when neededCarries out duties in compliance with established business policiesDemonstrates commitment to the development, implementation and effectiveness of Quality Management System per ISO, FDA, and other regulatory agenciesResponsible for exhibiting professional behavior with both internal/external business associates that reflects positively on the company and is consistent with the company's policies and practicesPerform other duties & projects as assignedUnderstands and is aware of the quality consequences which may occur from the improper performance of their specific job. Has awareness of device defects that may occur in their area of responsibility, including product design, verification and validation, manufacturing and testing activities

Aug 2015 - Aug 2018

Validation Qa/Qc Analyst Ii

American Peptide Company

Under minimal supervision, responsible for a variety of production and non-production functions in support of manufacturing goals.Ensure product quality in all manufacturing operations by being alert and observant to detect problems and/or potential problems with equipment or productResponsible for running in-process, raw material release, calibration, and experimental devices, notifying appropriate personnel of results and completing all associated documentationResponsible for scheduling of testing activitiesResponsible for training and the documenting of training for all testing personnelResponsible for the completeness and accuracy of manufacturing documents and lab notebooksResponsible for retrieving and compiling data associated with all device testing and notifying the appropriate personnel if results are not in complianceResponsible for inventory accuracy of all testing related materialsInitiate and investigate Non-conforming Material Reports, Planned Deviations and Unplanned deviations when neededCarries out duties in compliance with established business policiesDemonstrates commitment to the development, implementation and effectiveness of Quality Management System per ISO, FDA, and other regulatory agenciesResponsible for exhibiting professional behavior with both internal/external business associates that reflects positively on the company and is consistent with the company's policies and practicesPerform other duties & projects as assignedUnderstands and is aware of the quality consequences which may occur from the improper performance of their specific job. Has awareness of device defects that may occur in their area of responsibility, including product design, verification and validation, manufacturing and testing activities

Aug 2015 - Aug 2018

Co-Founder, Operations Director

Alphexa Labs

Responsible for oversight of clinical and commercial drug product testing, packaging, and labeling, l provide strategic direction, tactical oversight and technical expertise for the Operations group. Improve the operational systems, processes and policies in support of organizations mission -- specifically, support better management reporting, information flow and management, business process and organizational planning. Manage and increase the effectiveness and efficiency of Support Services (HR, IT and Finance), through improvements to each function as well as coordination and communication between support and business functions. Play a significant role in long-term planning, including an initiative geared toward operational excellence. Oversee overall financial management, planning, systems and controls. Management of agency budget in coordination with the Executive Director. Development of individual program budgets Invoicing to funding sources, including calculation of completed units of service. Payroll management, including tabulation of accrued employee benefits. Disbursement of checks for agency expenses. Organization of fiscal documents. Regular meetings with Executive Director around fiscal planning. Supervise and coach office manager on a weekly basis.

Apr 2016 - May 2017

Analytical Chemist

Gsk

Brentford, Middlesex, Gb

A laboratory position in which products are tested to meet and Check and maintain FDA standards using latest technology for chemical and physical testing standards to ensure product compliance. Involves mass testing of product using analytical chemistry and microbiology techniques. In a range of testing from physical to chemical analysis

Feb 2014 - Apr 2015

Paramedic

Carmel Parks And Recreation

Provided emergency medical services

Jul 2009 - Aug 2013
3 education records

Christopher Sime education

Bachelors, Biomedical/Medical Engineering

Hartwick College

Bs, Biochemistry

Stony Brook University

Associate'S Degree, Advanced Project Management

Stanford University
FAQ

Frequently asked questions about Christopher Sime

Quick answers generated from the profile data available on this page.

What company does Christopher Sime work for?

Christopher Sime works for KINOVATE LIFE SCIENCES, INC.

What is Christopher Sime's role at KINOVATE LIFE SCIENCES, INC?

Christopher Sime is listed as Senior Manager Quality Engineering at KINOVATE LIFE SCIENCES, INC.

What is Christopher Sime's email address?

AeroLeads has found 1 work email signal at @bachem.com for Christopher Sime at KINOVATE LIFE SCIENCES, INC.

Where is Christopher Sime based?

Christopher Sime is based in Carlsbad, California, United States while working with KINOVATE LIFE SCIENCES, INC.

What companies has Christopher Sime worked for?

Christopher Sime has worked for Kinovate Life Sciences, Inc, Nitto Denko Corporation, Argonaut Manufacturing Services Inc., Abbott, and Bachem.

How can I contact Christopher Sime?

You can use AeroLeads to view verified contact signals for Christopher Sime at KINOVATE LIFE SCIENCES, INC, including work email, phone, and LinkedIn data when available.

What schools did Christopher Sime attend?

Christopher Sime holds Bachelors, Biomedical/Medical Engineering from Hartwick College.

What skills is Christopher Sime known for?

Christopher Sime is listed with skills including Laboratory Equipment, Laboratory, Hplc, Organic Chemistry, Validation, Protein Purification, Microbiology, and Quality Assurance.

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